The effect of maltodextrin on the recovery of lung function with a spirometer and muscle strength with a handgrip dynamometer in gynaecological post laparotomy patients under general anaesthesia

The effect of maltodextrin on the recovery of lung function with a spirometer and muscle strength with a handgrip dynamometer in gynaecological post laparotomy patients under general anaesthesia : A Double-blind Randomized Controlled Trial

Status

Unknown

Phases

Phase 2

Study type

Interventional

Source

TCTR

Registry ID

TCTR20241208003

Enrollment

Registered

2024-12-08

Start date

2024-11-25

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

Forced expiratory volume in one second Forced vital capacity Handgrip strength Neutrophil-to-lymphocyte ratio Gynecological post-laparotomy patients under general anesthesia. Spirometry Forced Expiratory Volume (FEV1) Vital Capacity (FVC) Hand grip Strength Handgrip dynamometer Neutrophil-Lymphocyte Ratio (NLR) Maltodextrin

Interventions

Water with yellow-flavored syrup (400 ml) the night before surgery at 10:00 PM and water with the same syrup (200 ml) 2 hours before surgery,50 g of maltodextrin mixed with yellow-flavored syrup (400

Placebo Comparator Dietary Supplement,Active Comparator Dietary Supplement

Placebo,Maltodextrin

Eligibility

Sex/Gender

Female

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with ASA physical status I or II Patients with nutritional status classified as SGA A Normal gastrointestinal motility with no signs of obstruction METS score greater than 4 Hemoglobin level exceeding 10 g/dl

Exclusion criteria

Exclusion criteria: Patients with intellectual disabilities. Patients experiencing motor or sensory aphasia. Patients with a history of cerebrovascular disease. Patients diagnosed with acute retinal detachment. Patients suffering from upper respiratory tract infections. Patients with a history of diabetes mellitus who maintain normal random or fasting blood glucose levels but have discontinued diabetes treatment without a doctor's recommendation, or those with an HbA1c greater than seven percent within the past six months. Patients whose body mass index is categorized as underweight or obese. Patients who are unwilling to participate, as indicated by their refusal to provide informed consent

Design outcomes

Primary

Measure	Time frame
FEV1, FVC, Handgrip Strength 24 hours preoperative, 24 hours postoperative, 48 hours postoperative Spirometry, Handgrip strength test	—

Secondary

Measure	Time frame
neutrophil-to-lymphocyte ratio 24 hours preoperative, 24 hours postoperative complete blood count	—

Countries

Indonesia

Contacts

Public ContactChandra Gunawan

Faculty of Medicine Udayana University

crgbius2021@gmail.com081331731164

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026