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Effect of general anesthesia on sleep outcomes after minimally invasive urological surgery in patients with chronic insomnia: a randomized controlled study

Effect of general anesthesia on sleep outcomes after minimally invasive urological surgery in patients with chronic insomnia: a randomized controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076334
Enrollment
Unknown
Registered
2023-10-04
Start date
2023-08-24
Completion date
Unknown
Last updated
2023-10-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perioperative sleep outcome

Interventions

Deep sedation under general anesthesia group:State index (PSI) was monitored after the patient entered the room, propofol was used to maintain the PSI:20-35 until the end of the operation.
Light sedation under general anesthesia group:State index (PSI) was monitored after the patient entered the room, propofol was used to maintain the PSI:20-35 until the end of the operation.
Local anesthesia group:A single injection of lumbar anesthesia was performed.

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1, gender is not limited 2, age 18-75 years old, 18=BMI=28Kg/? / 3. ASA grade I-III 4. Patients requiring short urological operations and hospitalization 5, with basic reading and understanding skills, or clear questions and answers, can complete the scale survey with the help of medical personnel. 6. Patients who sign informed consent, voluntarily participate in this project and can complete relevant monitoring as required

Exclusion criteria

Exclusion criteria: 1, there are anxiety, depression and other mental diseases and other neurological diseases 2. Patients with severe physical diseases such as heart, lung, liver, and brain were considered unsuitable for this study 3, patients can not cooperate or can not adhere to treatment, predict patients with poor compliance 4. The patient is also participating in other clinical trials 5. For any other reason that the researcher deems it inappropriate to participate in this experimenter

Design outcomes

Primary

MeasureTime frame
Insomnia Severity Index;

Secondary

MeasureTime frame
Pittsburgh sleep quality index;Self-Rating Scale of Sleep;Deep sleep duration;Light sleep time;Rem sleep time;Improvement interview of Brice;Improvement interview of Likert scale;RBDSQ;3D-CAM;VAS;Incidence of urinary retention;The incidence of major postoperative complications;LOS;

Countries

China

Contacts

Public ContactCheng Xinqi

The First Affiliated Hospital of Anhui Medical University

ay_mz_cheng@126.com+86 139 6501 5671

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026