Nerve block during hysterectomy may boost post-surgery sleep quality
NCT ID NCT07069322
First seen Jul 08, 2026 · Last updated Jul 09, 2026 · Updated 1 time
Summary
This trial tests whether adding a regional nerve block (TAP or rectus sheath block) to general anesthesia helps women sleep better after a total abdominal hysterectomy. Sleep quality is measured using the Richards-Campbell Sleep Questionnaire. The study includes women aged 18–70 who are scheduled for elective surgery and can answer the questionnaire, but excludes those with sleep disorders or psychiatric conditions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- regional nerve block (TAP or rectus sheath block)
- What this could lead to
- If it works, this could point toward a simple way to help women sleep better after major gynecologic surgery.
- What could go wrong
- This is a small, early-stage trial with only 66 participants. The sleep improvement may be modest or not clinically meaningful, and results may not apply to other surgeries or populations.
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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66 people
The number who actually took part.
- Started
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Jul 2025
- Finished
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Dec 2025
- 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
Women between the ages of 18 and 70 who will undergo TAH operation under general anesthesia.
- Ages
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18 to 70 years
- Sex
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Female participants only
- Healthy volunteers
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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: * Elective TAH planned * ASA I-III group * Female patients aged 18-70 years * Those who are planned to be hospitalized at least one night in the postoperative period * Those who have the cognitive capacity to understand and answer the questionnaire Exclusion Criteria: * Patients with a history of neurological or psychiatric disease * Patients diagnosed with sleep disorders * Patients with sedative/hypnotic drug use * Patients requiring additional surgical intervention during the operation * Patients admitted to intensive care unit * Patients operated with epidural or spinal anesthesia
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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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Haseki Training and Research Hospital
Istanbul, Sultangazi, Turkey (Türkiye)