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Effect of Preoperative Oral Carbohydrate Administration in Thoracic Surgery Patients (oralcarbohydra)

I

Istanbul Sureyyapasa Chest Diseases and Chest Surgery Training and Research Hospital

Status

Completed

Conditions

Non Small Cell Lung Cancer
Postoperative Pneumonia
Fasting

Treatments

Dietary Supplement: Oral carbohydrate

Study type

Interventional

Funder types

Other

Identifiers

NCT05005091
SureyyapasaM

Details and patient eligibility

About

Preoperative carbohydrate loading has been shown to reduce pre-operative discomfort and postoperative nausea and vomiting. There is no need for prolonged preoperative fasting of the patients, but the traditional approach still continues especially in thoracic surgery patients. For this purpose, we aimed to evaluate the effect of preoperative carbohydrate loading on postoperative morbidity in the patients.

Full description

The study was conducted on 94 patients. The patients in the control group were fasting after midnight. Experimental group patients consumed carbohydrate drink as liquid two hours before the operation. 47 patients were in the control group (A) and 47 patients were in the experimental group (B). The groups were compared in terms of length of hospital and intensive care unit stay, vomiting, gas-stool outlet, postoperative pain conditions (VAS), inflammation parameters, blood glucose, and mobilization time.

SPSS 11.0 (SPSS, Inc., Chicago, IL, USA) was used for statistical analyses. All means were presented with 95% confidence limits. In the empirical analysis, t-test and chi-square test were used. In addition, correlation analysis was used to determine the relationship between fasting time and surgical recovery time.

Enrollment

94 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Stage I-Stage II all operable NSCLC patients -

Exclusion criteria

Patients with diabetes mellitus, a history of delayed gastric emptying, severe hepatic or renal failure, or any endocrine disorder that might influence the metabolic parameters were excluded, as were patients requiring urgent or emergent surgery.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

94 participants in 2 patient groups

oral carbohydrate
Active Comparator group
Description:
the patients drunk oral carbohydrate two hours ago preoperatively
Treatment:
Dietary Supplement: Oral carbohydrate
no oral carbohydrate
No Intervention group
Description:
the patients did not drink oral carbohydrate preoperatively

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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