NCT07562776

Brief Summary

This randomized controlled trial aims to compare the effect of preoperative carbohydrate loading versus standard overnight fasting on postoperative recovery time in patients undergoing elective abdominal surgery. A total of 144 admitted patients will be randomly assigned to either receive a preoperative carbohydrate drink or follow routine fasting protocols. The primary objective is to evaluate differences in postoperative recovery time between the two groups. Secondary outcomes include length of hospital stay, postoperative complications, and patient comfort. The findings of this study may help optimize preoperative fasting guidelines and improve patient recovery outcomes.

Trial Health

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Trial Health Score

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Enrollment
144

participants targeted

Target at P75+ for not_applicable

Timeline
16mo left

Started Oct 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 25, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 1, 2026

Completed
5 months until next milestone

Study Start

First participant enrolled

October 1, 2026

Expected
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2027

3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2028

Last Updated

May 1, 2026

Status Verified

April 1, 2026

Enrollment Period

1.1 years

First QC Date

April 25, 2026

Last Update Submit

April 25, 2026

Conditions

Keywords

ERAS protocolPre op carbohydrate loading doseLess time of npo

Outcome Measures

Primary Outcomes (1)

  • Post operative insuline resistance

    To evaluate the effect of preoperative oral carbohydrate loading compared with standard fasting on postoperative insulin resistance in patients undergoing elective abdominal surgery. Insulin resistance will be assessed by measuring fasting blood glucose and serum insulin levels preoperatively and postoperatively, and calculating insulin resistance using the Homeostatic Model Assessment for Insulin Resistance (HOMA-IR).

    24 hours after surgery

Secondary Outcomes (1)

  • Time to first oral intake

    24 hours after surgery

Study Arms (2)

Pre operative carbohydrate Loading group

EXPERIMENTAL

Patients in this group will receive a preoperative carbohydrate-rich clear liquid drink before elective abdominal surgery to reduce insulin resistance, improve postoperative recovery, and decrease discomfort associated with prolonged fasting.

Dietary Supplement: Patients will be given 400 mL of a carbohydrate-rich clear drink (10% daxtrosewater) approximately 2-3 hours before induction of anesthesia, according to ERAS guidelines.

Standard preoperative fasting group

ACTIVE COMPARATOR

Patients in this group will follow the routine preoperative fasting protocol as per hospital practice, including overnight fasting from solids and clear liquids according to standard anesthetic guidelines before elective abdominal surgery. No preoperative carbohydrate drink will be administered. Postoperative recovery outcomes will be compared with the intervention group receiving preoperative carbohydrate loading.

Other: Standard pre operative fasting

Interventions

Most previous studies have evaluated preoperative carbohydrate loading in mixed surgical populations or in settings outside Pakistan. Limited local data exist specifically for elective abdominal surgery patients in a single-center Pakistani tertiary care hospital setting. Thisstudy focuses on comparing a standardized carbohydrate loading dose with conventional fasting and assessing its direct impact on postoperative recovery time in your local population. surgery patients specifically It uses a standardized carbohydrate loading dose It compares against the routinely practiced prolonged fasting protocol It is conducted in a single-center local hospital population, where local evidence is limited It focuses on postoperative recovery time as the primary clinical outcome

Pre operative carbohydrate Loading group

Patients in this group will follow the routine preoperative fasting protocol according to hospital and anesthesia guidelines, including overnight fasting from solids and clear liquids before elective abdominal surgery. No preoperative carbohydrate loading will be give

Standard preoperative fasting group

Eligibility Criteria

Age20 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patients aged 20-60
  • ASA I-II classification.
  • Elective open or laparoscopic abdominal surgeries.

You may not qualify if:

  • Diabetes mellitus or impaired fasting glucose.
  • Emergency surgeries.
  • Patients with hepatic or renal dysfunction.
  • Patients on corticosteroids or insulin-sensitizing agents.
  • Pregnant patients.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Post graduate resident

Study Record Dates

First Submitted

April 25, 2026

First Posted

May 1, 2026

Study Start (Estimated)

October 1, 2026

Primary Completion (Estimated)

November 1, 2027

Study Completion (Estimated)

February 1, 2028

Last Updated

May 1, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share