Blood-Based injection may ease Post-Spinal headaches
NCT ID NCT06790758
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether an injection of plasma-rich fibrin (a substance made from the patient's own blood) could relieve severe headaches that sometimes occur after a spinal tap or epidural. Sixty adults with this type of headache received the injection through a special catheter. Researchers measured pain levels and how long patients needed bed rest, aiming to see if the treatment provides relief.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- plasma-rich fibrin
- What this could lead to
- If it works, this could offer a new treatment option for severe headaches caused by spinal fluid leaks.
- What could go wrong
- This is a small, completed study without a control group, so results may not be definitive. The procedure carries risks like infection or allergic reaction.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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60 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Nov 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age from 18 to 65 years. * Both sexes. * Patients suffering from severe post-dural puncture headache. Exclusion Criteria: * Uncooperative patients. * Severe comorbid conditions. * Pregnancy. * Anticoagulant therapy. * Known allergies to plasma rich fibrin components. * Body mass index (BMI) ≥35 kg/m2.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Tanta University
Tanta, El-Gharbia, 31527, Egypt
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