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to compare two types of warming blankets for prevention of hypothermia during colorectal surgery

Comparison of two Forced air warming blankets for prevention of intraoperative hypothermia in colorectal surgeries: A prospective randomized study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/06/019576
Enrollment
60
Registered
2019-06-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: C189- Malignant neoplasm of colon, unspecified

Interventions

Intervention1: Under-body forced Air warming Blanket: This is a forced air warming blanket that is placed under the patient and connected to the warming device. The blanket will be placed immediately

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18-65 years of both sexes 2.Patients belonging to American Society of Anesthesiologists (ASA) Grade I & II 3.Patients scheduled for elective carcinoma colorectal surgeries.

Exclusion criteria

Exclusion criteria: 1. Patients with uncontrolled hypertension and coronary artery disease. 2. Patients with morbid obesity BMI >40kg/m2). 3. Preoperative body temperature >37.5°C 4. Surgeries lasting less than 2 hours.

Design outcomes

Primary

MeasureTime frame
To study the average intraoperative temperature values in both the groups.Timepoint: the temperature will be recorded every 10 minutes from start of surgery to end of surgery

Secondary

MeasureTime frame
To study intraoperative hemodynamic parameters in the form of MBP, heart rate. To study intraoperative use of amount of fluids, blood products and opioids. To study Platelet and coagulation pathway as tested by thromo-elastography. Study postoperative recovery times (Aldrete score9) To study postoperative incidence of any shivering or sweating in the two groups. To study any other adverse effect in any of the patients. Timepoint: all hemodynamic will be recorded every 10 minutes. total, fluids, blood products and opioids will be recorded at the end of surgery the TEG will be recorded baseline and at the end of surgery Aldrett score and shivering will be recorded at the end of surgery

Countries

India

Contacts

Public ContactNISHKARSH GUPTA

DRBRAIRCH, AIIMS

drnishkarsh@rediffmail.com09013310014

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026