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Recruiting NCT06818942

Nomogram for Predicting Difficult Laparoscopic Appendectomy

Observational Emergencies

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Observations on preoperative and intraoperative factors influencing the difficulty of surgery.
Who it may be relevant to
Registry conditions: Emergencies. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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.

Detailed description

Acute appendicitis is the most common cause of surgical emergencies and laparoscopic appendectomy (LA) is usually attempted by surgical trainees. This study aim to explore the preoperative and intraoperative factors affecting the degree of surgical difficulty and to establish a model for validation, so that it can be subsequently replicated in training programs.

Interventions

  • Other 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

Primary outcome measures

  • Operative time [Time frame: During surgery]
  • Number of participants with postoperative complications [Time frame: through study completion, an average of 1 year]
  • Hospitalization [Time frame: 1 day of discharge]
  • Degree of pain [Time frame: approximately 4 hours after surgery and on postoperative day 1]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Shanghai Sixth People's Hospital — Shanghai

Identifiers

NCT: NCT06818942 · 2025-KY-094(K)

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗