Inherited renal tubular disease
MONDO:0015962Also known as: genetic renal tubular disease
41 clinical trials for this condition and its sub-types, 0 tagged with Inherited renal tubular disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Inherited renal tubular disease
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Pseudohypoparathyroidism 8 trials · 9 incl. sub-types
5 sub-types
- Pseudohypoparathyroidism type 1A 7 trials
- Pseudopseudohypoparathyroidism 2 trials
- Pseudohypoparathyroidism type 1B 0 trials
- Pseudohypoparathyroidism type 1C 0 trials
- Pseudohypoparathyroidism type 2 0 trials
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Cystinuria 7 trials
2 sub-types
- Cystinuria type A 0 trials
- Cystinuria type B 0 trials
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Dent disease 5 trials
2 sub-types
- Dent disease type 1 0 trials
- Dent disease type 2 0 trials
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Familial primary hypomagnesemia 5 trials
5 sub-types
- Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis 0 trials · 1 incl. sub-types Sub-types →
- EGF-related primary hypomagnesemia with intellectual disability 0 trials
- Familial primary hypomagnesemia with hypocalcuria 0 trials Sub-types →
- Familial primary hypomagnesemia with normocalcuria 0 trials Sub-types →
- Hypomagnesemia 7, renal, with or without dilated cardiomyopathy 0 trials
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Nephronophthisis 4 trials
18 sub-types
- Nephronophthisis 1 4 trials
- Late-onset nephronophthisis 0 trials
- Nephronophthisis 11 0 trials
- Nephronophthisis 12 0 trials
- Nephronophthisis 13 0 trials
- Nephronophthisis 14 0 trials
- Nephronophthisis 15 0 trials
- Nephronophthisis 16 0 trials
- Nephronophthisis 18 0 trials
- Nephronophthisis 19 0 trials
- Nephronophthisis 2 0 trials
- Nephronophthisis 20 0 trials
- Nephronophthisis 3 0 trials
- Nephronophthisis 4 0 trials
- Nephronophthisis 7 0 trials
- Nephronophthisis 9 0 trials
- Nephronophthisis-like nephropathy 1 0 trials
- Nephronophthisis-like nephropathy 2 0 trials
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Oculocerebrorenal syndrome 3 trials
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Hereditary renal hypouricemia 2 trials
3 sub-types
- Hypouricemia, renal 1 trial · 2 incl. sub-types Sub-types →
- Hypouricemia, familial renal, due to tubular hypersecretion 0 trials
- Hypouricemia, hypercalcinuria, and decreased bone density 0 trials
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Jeune syndrome 1 trial · 2 incl. sub-types
24 sub-types
- Ellis-van Creveld syndrome 1 trial Sub-types →
- Beemer-Langer syndrome 0 trials
- Jeune syndrome - GRK2-related 0 trials
- Asphyxiating thoracic dystrophy 1 0 trials
- Asphyxiating thoracic dystrophy 2 0 trials
- Asphyxiating thoracic dystrophy 3 0 trials
- Asphyxiating thoracic dystrophy 4 0 trials
- Asphyxiating thoracic dystrophy 5 0 trials
- Short-rib thoracic dysplasia 10 with or without polydactyly 0 trials
- Short-rib thoracic dysplasia 11 with or without polydactyly 0 trials
- Short-rib thoracic dysplasia 13 with or without polydactyly 0 trials
- Short-rib thoracic dysplasia 14 with polydactyly 0 trials
- Short-rib thoracic dysplasia 15 with polydactyly 0 trials
- Short-rib thoracic dysplasia 16 with or without polydactyly 0 trials
- Short-rib thoracic dysplasia 17 with or without polydactyly 0 trials
- Short-rib thoracic dysplasia 18 with polydactyly 0 trials
- Short-rib thoracic dysplasia 19 with or without polydactyly 0 trials
- Short-rib thoracic dysplasia 20 with polydactyly 0 trials
- Short-rib thoracic dysplasia 21 without polydactyly 0 trials
- Short-rib thoracic dysplasia 22 without polydactyly 0 trials
- Short-rib thoracic dysplasia 6 with or without polydactyly 0 trials
- Short-rib thoracic dysplasia 7 with or without polydactyly 0 trials
- Short-rib thoracic dysplasia 8 with or without polydactyly 0 trials
- Short-rib thoracic dysplasia 9 with or without polydactyly 0 trials
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Senior-Loken syndrome 1 trial · 2 incl. sub-types
9 sub-types
- Senior-Loken syndrome 1 1 trial
- Senior-Loken syndrome 4 0 trials
- Senior-Loken syndrome 5 0 trials
- Senior-Loken syndrome 6 0 trials
- Senior-Loken syndrome 7 0 trials
- Senior-Loken syndrome 8 0 trials
- Senior-Loken syndrome 9 0 trials
- Nephronophthisis 15 0 trials
- Senior-loken syndrome 3 0 trials
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Nephrogenic diabetes insipidus 1 trial · 2 incl. sub-types
2 sub-types
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Pseudohypoaldosteronism type 1 1 trial · 2 incl. sub-types
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EAST syndrome 1 trial
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HELIX syndrome 1 trial
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RHYNS syndrome 1 trial
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Bartter syndrome 0 trials
6 sub-types
- Bartter disease type 1 0 trials
- Bartter disease type 2 0 trials
- Bartter disease type 3 0 trials
- Bartter disease type 5 0 trials
- Bartter syndrome type 4 0 trials Sub-types →
- Bartter syndrome with hypocalcemia 0 trials
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Gitelman syndrome 0 trials
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Senior-Boichis syndrome 0 trials
1 sub-type
- Nephronophthisis 11 0 trials
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Cranioectodermal dysplasia 0 trials
7 sub-types
- Cranioectodermal dysplasia 1 0 trials
- Cranioectodermal dysplasia 2 0 trials
- Cranioectodermal dysplasia 3 0 trials
- Cranioectodermal dysplasia 4 0 trials
- Cranioectodermal dysplasia 5 0 trials
- Cranioectodermal dysplasia 6 0 trials
- Short-rib thoracic dysplasia 16 with or without polydactyly 0 trials
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3 sub-types
Most studied deeper sub-types
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Old asthma drug shows promise for rare genetic disorder
Disease control OngoingThis phase 2 trial tests whether theophylline, a drug used for asthma, can help people with pseudohypoparathyroidism lose weight and improve blood sugar control. The study includes 29 obese participants aged 13 and older. Researchers will measure changes in body mass index and gl…
Phase 2 • Sponsor: Vanderbilt University Medical Center • Aim: Disease control
Last updated Sep 04, 2026 00:00 UTC
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Could a common asthma drug help treat a rare genetic disorder?
Disease control By invitation onlyThis study tests whether theophylline, a drug used for asthma, can help children and young adults with pseudohypoparathyroidism—a rare genetic condition causing early obesity, hormone problems, and short stature. Researchers will check for weight loss, better blood sugar control,…
Phase 2 • Sponsor: Jaclyn Tamaroff • Aim: Disease control
Last updated Sep 04, 2026 00:00 UTC
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Single-Patient trial aims to tackle obesity in rare bone disorder
Disease control By invitation onlyThis phase 2 trial tests the drug setmelanotide in one person with pseudohypoparathyroidism type 1a (PHP1a), a rare genetic disorder that often causes severe obesity. The participant will receive daily injections of setmelanotide for six months to see if it leads to weight loss a…
Phase 2 • Sponsor: Massachusetts General Hospital • Aim: Disease control
Last updated Jul 25, 2026 00:00 UTC
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Experimental cocktail aims to silence Life-Threatening food allergies
Disease control OngoingThis early-stage study tests two drugs together—linvoseltamab and dupilumab—in just 6 adults with severe food allergies. The goal is to see if the combination is safe and can lower IgE antibodies that trigger allergic reactions. Participants must have a history of anaphylaxis to …
Phase 1 • Sponsor: Regeneron Pharmaceuticals • Aim: Disease control
Last updated Jun 28, 2026 00:00 UTC
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Old asthma drug could help kids with rare bone and hormone disorder
Disease control OngoingThis phase 2 trial tests theophylline, a drug used for asthma, in 34 children aged 2 to 12 with pseudohypoparathyroidism, a genetic condition causing obesity, short stature, and hormone resistance. The study aims to see if theophylline can help with weight loss, slow bone growth …
Phase 2 • Sponsor: Vanderbilt University Medical Center • Aim: Disease control
Last updated Jun 27, 2026 12:24 UTC
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Cystinuria drug trial pulled before it even started
Disease control CancelledThis study was designed to test whether ADV7103, a combination of potassium citrate and potassium bicarbonate, could help people with cystinuria by making their urine less acidic. The goal was to see if it could raise urine pH to 7.0 or higher, which might reduce kidney stone for…
Phase 2/3 • Sponsor: Advicenne Pharma • Aim: Disease control
Last updated Jun 27, 2026 08:09 UTC
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Newborn screening study aims to catch rare diseases at birth
Diagnosis OngoingThis study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…
Sponsor: RTI International • Aim: Diagnosis
Last updated Jul 03, 2026 00:00 UTC
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Magnesium-Rich diet may prevent chemo side effect in ovarian cancer
Prevention OngoingThis study looks at whether eating a diet high in magnesium can help prevent low blood magnesium levels in women with ovarian cancer who are receiving carboplatin chemotherapy. Low magnesium is a common side effect of this treatment. The study enrolled 26 participants and will me…
Sponsor: M.D. Anderson Cancer Center • Aim: Prevention
Last updated Aug 23, 2026 00:00 UTC
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Could a simple supplement shield bones and kidneys from common heartburn drugs?
Prevention CancelledThis trial investigates whether a daily effervescent supplement containing calcium, magnesium, and citrate can prevent bone loss, magnesium deficiency, and kidney damage in adults who take proton pump inhibitors (PPIs) long-term for conditions like heartburn or GERD. Participants…
Phase 3 • Sponsor: University of Texas Southwestern Medical Center • Aim: Prevention
Last updated Jul 02, 2026 00:00 UTC
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Sound waves may replace X-Rays for dental implant timing
Knowledge-focused OngoingThis study at the University of Michigan is testing whether ultrasound can monitor bone graft healing after tooth extraction, potentially replacing more invasive scans. About 140 adults needing a tooth extraction and bone graft for a future dental implant will have their healing …
Sponsor: University of Michigan • Aim: Knowledge-focused
Last updated Sep 16, 2026 00:00 UTC
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Ground-Level vision test could help retinitis pigmentosa patients walk better
Knowledge-focused CancelledThis study was designed to see if a new method of measuring the visual field—by projecting vision zones on the ground—helps people with retinitis pigmentosa understand their remaining sight and improve their walking rehabilitation. The trial was withdrawn before enrolling any par…
Sponsor: University Hospital, Limoges • Aim: Knowledge-focused
Last updated Jun 27, 2026 13:05 UTC
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Long-Term study sheds light on rare bone and hormone disorder
Knowledge-focused OngoingThis study follows 600 people with Albright hereditary osteodystrophy, a rare genetic condition affecting bones and hormones. Researchers are looking at how growth hormone treatment affects height and weight in those with a related hormone problem, and also studying thinking and …
Sponsor: Connecticut Children's Medical Center • Aim: Knowledge-focused
Last updated Jun 27, 2026 13:01 UTC
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Study probes Patients' minds, not their tumors
Knowledge-focused OngoingThis study looks at how older adults (65+) with cancer understand their illness and what they value in life before and after a major operation. Researchers will interview 100 patients to learn about their awareness, expectations, and decision-making. No new drug or treatment is b…
Sponsor: Tomas Bata Hospital, Czech Republic • Aim: Knowledge-focused
Last updated Jun 27, 2026 11:02 UTC