Not Yet RecruitingNot Applicable

The Role of Regional Analgesia in Sleep Quality

66 participantsStarted 2025-07-25

Plain-language summary

To evaluate the effect of regional analgesic blocks (TAP or rectus sheath block) applied in addition to general anesthesia on postoperative sleep quality in patients undergoing total abdominal hysterectomy (RCSQ score).

Who can participate

Age range

18 Years – 70 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Richards-Campbell Sleep Questionnaire Score (RCSQ)

Timeframe: Postoperative 24 hours

Trial details

NCT IDNCT07069322

SponsorHaseki Training and Research Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-11-25

Contact for this trial

Ali Çetin

905422723113 dralicetin@yahoo.com

View on ClinicalTrials.gov More Richards-Campbell Sleep Questionnaire (RCSQ) trials