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Recruiting Observational

Nomogram for Predicting Difficult Laparoscopic Appendectomy

NCT06818942 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2025-01-26
Last updated
2026-05-07

Condition(s) studied

Emergencies

Investigational drug(s) / intervention(s)

Observations on preoperative and intraoperative factors influencing the difficulty of surgery

Observations on preoperative and intraoperative factors influencing the difficulty of surgery: Age, body mass index, gender, inflammatory indicators, previous history of abdominal surgery, underlying disease

Study summary

No prior studies have stratified the difficulty of laparoscopic appendectomy (LA). The investigators aimed to investigate preoperative factors as indicators of difficult LAs based on the experience of surgical trainees and to develop a predictive model accordingly.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Clinical diagnosis of acute appendicitis * Participants who underwent laparoscopic appendectomy Exclusion Criteria: * Participants refused or could not tolerate laparoscopic appendectomy * Incomplete preoperative examination or missed information

Primary outcome measure(s)

  • Operative time — During surgery
    operative time was defined as the duration from incision to closure, and was collected from anesthesia record sheet
  • Number of participants with postoperative complications — through study completion, an average of 1 year
    Postoperative bleeding, surgical site infection and other complications
  • Hospitalization — 1 day of discharge
    days of hospitalization
  • Degree of pain — approximately 4 hours after surgery and on postoperative day 1
    pain intensity was assessed using a standard visual analogue score, with a score of 0 to 10 corresponding to no pain to the most severe pain

Trial sites (1)

FacilityCityRegionStatus
Shanghai Sixth People's Hospital Shanghai Shanghai Municipality Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06818942 on ClinicalTrials.gov ↗ ← All trials in China