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Impact of ERAS Protocol on Length of Hospital Stay After Laparoscopic Surgeries

Impact of Multimodal Analgesia and ERAS Protocol on Length of Hospital Stay After Laparoscopic Gynecological Surgeries: A Randomized Control Trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07116564
Enrollment
98
Registered
2025-08-11
Start date
2025-08-20
Completion date
2026-11-01
Last updated
2026-02-17

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

Conditions

ERAS

Brief summary

The goal of this clinical trial is to determine the length of hospital stay in patients using multimodal analgesia with or without ERAS protocol scheduled for elective laparoscopic gynecological surgeries

Interventions

DRUGEnhanced Recovery After Surgery

Preoperatively ERAS protocol includes, No solid food for 6 hours before procedure; 800 ml (fantomalt powder) Carbohydrate drink 8 hours before surgery; 400 ml (fantomalt powder) 2 hours before surgery; Celecoxib 200g 1 hour before surgery . Intraoperatively, on induction lidocaine 1.5 mg/kg and Fentanyl 1 to 2 mcg/kg followed by IV lidocaine infusion at 1.5 mg/kg/h.

DRUGControl

Preoperatively, NPO 6 hours before the procedure Intraoperatively, on induction Nabuphine 0.1mg/kg

Sponsors

Aga Khan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* ASA physical status I, II, and III * Patients scheduled for elective laparoscopic gynecological surgeries

Exclusion criteria

* Refusal to participate * History of allergy or contraindication to study drugs * Patients in which procedure converted to open surgery * Diagnostic laparoscopic procedures * Patients with a history of severe anxiety or depression

Design outcomes

Primary

MeasureTime frameDescription
Length of hospital stayFrom arrival in the recovery room post-surgery until 72 hours after surgery.Post-operative length of hospital stay, measured in hours from the patient's arrival in the recovery room until 72 hours after surgery.

Secondary

MeasureTime frameDescription
Postoperative pain score4 hours, 8 hours, 12 hours, 24 hours, 48 hours & 72 hours postoperativelyPost operative pain score will be measures using NRS (Numerical Rating Scale). Eleven points pain scale measures from 0-10, where "0" is no pain and "10" is the worst possible pain
Amount of opioid used in patient controlled analgesia12 hours postoperatively.Total Nalbuphine consumption in 12 hours (in milligrams)
Patient satisfaction Score24 hours after the operationPatient satisfaction with the pain management regimen will be assessed using a five-point Likert scale 24 hours after surgery. The scale ranges from 1 to 5, where 1 = Very Dissatisfied, 2 = Dissatisfied, 3 = Neutral, 4 = Satisfied, and 5 = Very Satisfied. Higher scores indicate greater satisfaction.

Countries

Pakistan

Contacts

CONTACTAli Sarfraz Siddiqui, MBBS, MCPS, FCPS, FIPP, MHPE
sarfraz.siddiqui@aku.edu+922134864397

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026