Clinical trial Recruiting at 1 site Interventional Ages 60 and up

Maltodextrin vs Sugar Water for Pre-Surgery Carbohydrate Loading in Older Adults

Official title: Comparison of Maltodextrin and Sugar Water Carbohydrate Loading on Gastric Volume in Geriatric Patients Undergoing Lower Extremity Orthopedic Surgery

Run by Udayana University · NCT07872683 · Data updated 2026-11-12

This study tests whether a maltodextrin drink before surgery leaves less fluid in the stomach than sugar water for adults 60 and older undergoing leg surgery with spinal or epidural anesthesia.

Quick facts

Study typeInterventional
Ages60 Years and up
SexAll
Enrollment62 (estimated)
SponsorUdayana University
Academic / other
Locations1 site (Denpasar, Bali)
StatusRecruiting
StartedSeptember 27, 2026
Main results expectedOctober 31, 2026
Study endsNovember 30, 2026
Registry record updatedOctober 14, 2026
Trial IDNCT07872683 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults 60+ with ASA II or III status, undergoing elective lower limb orthopedic surgery under neuraxial anesthesia, and able to consent with adequate cognitive function.

Probably not a fit

Patients with gastrointestinal pathology, recent bariatric surgery, or conditions affecting gastric emptying may not benefit and could be excluded.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized, double-blind trial compares two preoperative carbohydrate drinks in adults aged 60 and above scheduled for elective lower limb orthopedic surgery under neuraxial anesthesia. Participants receive 400 mL of either maltodextrin or sugar water 2 hours before anesthesia, with gastric volume measured by ultrasound and blood glucose monitored at specified times. The study aims to see which drink alters gastric fluid and glucose responses more favorably, within a controlled, parallel-group design. Outcomes include gastric volume before and after drinking, and glucose levels up to 6 hours post-surgery, alongside basic perioperative data. The trial is conducted at a hospital in Denpasar, Indonesia, with double-blinding maintained through identical containers and labeling.

Why it matters

Potential benefit: If maltodextrin reduces gastric volume or stabilizes glucose better, patients could experience safer anesthesia induction and smoother recovery.

How similar studies have gone: Prior ERAS-focused studies support carbohydrate loading, but direct comparison between maltodextrin and sugar water in this age group is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 60 years or older with adequate cognitive function on brief cognitive screening
* ASA physical status II or III
* Elective lower extremity orthopedic surgery under neuraxial anesthesia

Exclusion Criteria:

* Emergency or urgent surgery
* Unstable hemodynamics
* Diagnosed gastrointestinal tract pathology
* History of bariatric surgery
* Dressing, wound cover or corset over the abdomen that prevents gastric ultrasound
* Use of a proton pump inhibitor, H2 antagonist or drug affecting gastrointestinal motility (for example metoclopramide, loperamide) in the past week
* Unable to lie in the lateral decubitus position
* Body mass index below 19 or 35 kg/m2 and above
* Refuses to take part after informed consent

Where it's running

  • Prof. Dr. I.G.N.G. Ngoerah General Hospital (RSUP Prof. Dr. I.G.N.G. Ngoerah)
    Denpasar, Bali, Indonesia
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.