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Optimizing postoperative rehabilitation for female surgical patients: a new treatment strategy for postoperative sleep and pain management

Optimizing postoperative rehabilitation for female surgical patients: a new treatment strategy for postoperative sleep and pain management

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108204
Enrollment
Unknown
Registered
2025-08-26
Start date
2025-09-28
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Postoperative sleep disorders and pain management in women

Interventions

Trial group:After the surgery, immediately initiate the postoperative analgesia program, using sufentanil 2.0ug/kg+dexmedetomidine 3ug/kg+tropisetron 8mg. The analgesia pump setting scheme is: no load
Control group:After the surgery, immediately initiate the postoperative analgesia program, using sufentanil 2.0ug/kg+tropisetron 8mg. The analgesia pump setting scheme is: no loading dose, continuous

Sponsors

Xishuangbanna Dai Autonomous Prefecture People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1 All female patients who undergo elective surgical procedures; 2 Age range: 18-65 years old; 3 18.5kg/m^2 <= Body Mass Index (BMI) <= 30kg/m^2; 4 American Society of Anesthesiologists (ASA) physical status classification I-II; 5 Voluntarily participate and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Long-term use of sedative/analgesic drugs or history of chronic pain prior to surgery; 2. Severe cardiopulmonary diseases (e.g., sick sinus syndrome, atrioventricular block, severe sinus bradycardia (HR = 5 points; 6. Pregnant or breastfeeding women; 7. Intraoperative blood loss >= 500 ml or surgery duration >= 2 hours

Design outcomes

Secondary

MeasureTime frame
Pittsburgh Sleep Quality Index;Postoperative pain intensity;The number of presses of the analgesic pump within 48 hours after surgery (postoperative opioid consumption);Insufficient analgesia, rescue analgesia;Adverse reactions during postoperative analgesia (bradycardia, hypotension, nausea and vomiting);

Primary

MeasureTime frame
Incidence of postoperative sleep quality disorders (number of people with Pittsburgh sleep quality score > 5);

Countries

China

Contacts

Public ContactZeng Yi

Xishuangbanna Dai Autonomous Prefecture People's Hospital

uluem21@qq.com+86 139 8817 2889

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 7, 2026