Skip to content

Effect of Preoperative Oral Carbohydrate Administration in Thoracic Surgery Patients

Effect of Preoperative Oral Carbohydrate Administration in Thoracic Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05005091
Acronym
oralcarbohydra
Enrollment
94
Registered
2021-08-13
Start date
2017-01-01
Completion date
2018-04-30
Last updated
2021-08-13

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

Conditions

Fasting, Non Small Cell Lung Cancer, Postoperative Pneumonia

Keywords

Preoperative fasting, postoperative morbidity, preoperative carbohydrate drinking, thoracic surgery

Brief summary

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.

Detailed 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.

Interventions

DIETARY_SUPPLEMENTOral carbohydrate

100 ml oral carbohydrate two hours ago preoperatively

Sponsors

Istanbul Sureyyapasa Chest Diseases and Chest Surgery Training and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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. \-

Design outcomes

Primary

MeasureTime frameDescription
Mobilization time1 hourpostoperative mobilization

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026