Efficacy of IV Fluid Warmer for the Prevention of Hypothermia

NCT ID: NCT07192224

Last Updated: 2025-09-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

84 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-03-01

Study Completion Date

2025-09-02

Brief Summary

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This study focuses on the importance of the maintenance of body temperature during the surgeries. This study involves the comparison of 2 groups, one receiving warm fluids while the other group receiving room temperature fluids during surgeries.

Detailed Description

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This study focuses on the importance of the maintenance of body temperature during the surgeries. This study involves the comparison of 2 groups, one receiving warm fluids while the other group receiving room temperature fluids during surgeries.

Conditions

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Hypothermia Shivering

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Hotline

These patients had fluid via hotline.

Group Type EXPERIMENTAL

Hotline

Intervention Type DEVICE

Used as a fluid warmer.

Placebo

Received fluid at room temperature.

Group Type PLACEBO_COMPARATOR

Hypothermia

Intervention Type DEVICE

This study involves the comparison of 2 groups, one receiving warm fluids while the other group receiving room temperature fluids during surgeries.

Interventions

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Hypothermia

This study involves the comparison of 2 groups, one receiving warm fluids while the other group receiving room temperature fluids during surgeries.

Intervention Type DEVICE

Hotline

Used as a fluid warmer.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Age 18-60 years,
2. ASA I-II,
3. both Male \& female,
4. elective gastrointestinal cancer surgery -

Exclusion Criteria

1. Preoperative core temperature greater than 37.2,
2. severe endocrine respiratory \& cardiovascular disease. -
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shaukat Khanum Memorial Cancer Hospital & Research Centre

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Shaukat Khanam Memorial Cancer Hospital LAHORE

Lahore, Punjab Province, Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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IRB-23-03

Identifier Type: -

Identifier Source: org_study_id

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