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Preoperative pain and negative mood assessment in predicting pain after laparoscopic total hysterectomy

Preoperative pain and negative mood assessment in predicting pain after laparoscopic total hysterectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092339
Enrollment
Unknown
Registered
2024-11-14
Start date
2024-11-15
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Pain

Interventions

Group L:HADS=9 points
Group H:HADS >9 points
Group HI:VAS = 3 points
Group LI:VAS < 3 points

Sponsors

The First Affiliated Hospital, Jinan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Clearly conscious, able to tolerate surgical treatment, signed informed consent; 2.ASA grade I-II, age 35-65 years, BMI 18-30 kg/m2; 3.able to understand and independently complete the assessment scale; 4.no obvious anesthesia-related contraindications;

Exclusion criteria

Exclusion criteria: 1.Patients with severe preoperative cardiac, hepatic, or renal abnormalities; 2.patients on long-term nonsteroidal anti-inflammatory drugs (NSAIDs), chronic pain, or preoperative opioids; 3.those with allergies to opioids or medications used intraoperatively; 4.those with a history of drug or alcohol addiction; 5.patients with an unsuccessful primary venipuncture or peripheral vascular disease; 6.those who refused to undergo a General Hospital Anxiety and Depression Scale (HADS) score; 7.those who underwent mid-operative conversion to an open procedure; 8.and those who failed to complete the HADS scores or pain scores for those;

Design outcomes

Primary

MeasureTime frame
degree of pain;

Secondary

MeasureTime frame
Post-operative analgesic requirements;

Countries

China

Contacts

Public ContactYalan Li

The First Affiliated Hospital, Jinan University

13500013993@139.com+86 20 38688200

Outcome results

None listed

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