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Nomogram for Predicting Difficult Laparoscopic Appendectomy

Nomogram for Predicting Difficult Laparoscopic Appendectomy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06818942
Enrollment
500
Registered
2025-02-11
Start date
2025-01-26
Completion date
2027-12-31
Last updated
2026-05-07

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

Conditions

Emergencies

Keywords

Laparoscopic appendectomy, Surgical difficulty, Training program

Brief 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.

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

OTHERObservations on preoperative and intraoperative factors influencing the difficulty of surgery

Age, body mass index, gender, inflammatory indicators, previous history of abdominal surgery, underlying disease

Sponsors

Shanghai 6th People's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
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

Design outcomes

Primary

MeasureTime frameDescription
Operative timeDuring surgeryoperative time was defined as the duration from incision to closure, and was collected from anesthesia record sheet
Number of participants with postoperative complicationsthrough study completion, an average of 1 yearPostoperative bleeding, surgical site infection and other complications
Hospitalization1 day of dischargedays of hospitalization
Degree of painapproximately 4 hours after surgery and on postoperative day 1pain 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

Countries

China

Contacts

CONTACTLing Zhan, Dr
rebecca0428zhan@163.com08615821120972

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 8, 2026