Effect of cold bag on pain relief

Effect of cold therapy on pain, ventilation, oxygenation and hemodynamic parameters in patients undergoing coronary artery bypass graft surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201201038600N1

Enrollment

Registered

2012-02-14

Start date

2011-08-16

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

coronary artery bypass graft. atherosclerotic cardiovascular disease

Interventions

Intervention 1: Control group (without cold pack method): Not using cold pack (no intervention) before the first and second stages. Intervention 2: Intervention group (with ice bag method): Not using

Control group (without cold pack method): Not using cold pack (no intervention) before the first and second stages.

Intervention group (with ice bag method): Not using cold pack (no intervention) before the first stage and Using cold pack on sternotomy dressing for 20 minutes before the second stage.

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients undergoing CABG by sternotomy. Exclusion criteria: Allergic or sensitivity to cold, cognitive impairments, having chest tube at the time of data collection, developing severe post-op complication and receiving pain medications

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: numerical rating scale.;Sistolic and diastolic blood pressure. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: analogue manometer.;Pulse. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: By touching and counting pulse.;Maximum inspiratory volume. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: incentive spirometry.;Arterial o2 suturation. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: pulse oximetry.;Respiratory rate. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: By counting.	—

Measure

Time frame

Pain. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: numerical rating scale.;Sistolic and diastolic blood pressure. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: analogue manometer.;Pulse. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: By touching and counting pulse.;Maximum inspiratory volume. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: incentive spirometry.;Arterial o2 suturation. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: pulse oximetry.;Respiratory rate. Timepoint: 2 stages with two hour interval between them in any method. Method of measurement: By counting.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactFahimeh Soltani Shirazi

Shiraz University of Medical Sciences

Soltanif@Sums.ac.ir , Far15us@yahoo.com+98 71 1647 4255

Outcome results

None listed

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