Could painkillers quietly disrupt your hormones?
NCT ID NCT01543425
First seen Aug 10, 2026 · Last updated Aug 11, 2026 · Updated 1 time
Summary
This study looks at whether chronic neuropathic pain and the medications used to treat it—like antidepressants, antiepileptics, or opioids—are linked to changes in hormone levels. Researchers will compare hormone levels in 120 adults with chronic pain to healthy volunteers matched by age, sex, and body size. The goal is to see if these hormonal changes might help explain why many pain patients report a lower quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If this study finds that certain pain medications disrupt hormone levels, it could point toward ways to improve quality of life for people with chronic pain.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. The findings may not apply to all pain patients, and the results are only a snapshot of hormone levels at one time.
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.
- Participants
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120 people
The number who actually took part.
- Start date
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Mar 2012
- Finished
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May 2013
- Lead sponsor
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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.
Who is studied
Patients older than 18 years, * Male or Female with BMI between 18 and 35, * Patients with chronic neuropathic pain for more than six months, except to diabetes or central neuropathic pain * Patients receiving systemic therapy for treating chronic neuropathic pain such as antidepressants, anticonvulsants or opiates for at least 6 months. Group of healthy volunteers * non-painful healthy volunteers matched by age, sex, BMI and menopausal status for women, * Free of analgesics within 8 days before the test, * Aged over 18 years, * Male or Female,
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Group of patients * Patients older than 18 years, * Male or Female with BMI between 18 and 35, * Patients with chronic neuropathic pain for more than six months, except to diabetes or central neuropathic pain * Patients receiving systemic therapy for treating chronic neuropathic pain such as antidepressants, anticonvulsants or opiates for at least 6 months. Group of healthy volunteers * non-painful healthy volunteers matched by age, sex, BMI and menopausal status for women, * Free of analgesics within 8 days before the test, * Aged over 18 years, * Male or Female, Exclusion Criteria: * Subjects with a medical history and / or surgical judged by the investigator or his representative as being incompatible with the test * Patients treated only by topical treatment (lidocaine patch only for example) * Pateints receiving corticosteroid treatment at the time of enrollment, or who received such treatment during the last 6 months (regardless of the dosage form and dosage), * Inflammatory and evolutive pathology requiring long term treatment, * Type 2 diabetes, * Postmenopausal women with replacement therapy, * Weight change of more than 5% within 3 months before the study, * BMI \<18 or\> 35,
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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
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CHU Clermont-Ferrand
Clermont-Ferrand, 63003, France
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Other studies related to the condition(s) this trial covers.
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