NCT07098962

Brief Summary

This study investigates the effectiveness of KinesioTaping applied around mediastinal and thoracic drain sites in reducing postoperative pain after cardiac surgery. Effective pain management is critical for early mobilization, improved patient satisfaction, and prevention of respiratory complications such as atelectasis. KinesioTaping is theorized to support soft tissue healing, improve circulation, and modulate pain through stimulation of cutaneous mechanoreceptors and fascia adjustment. However, evidence on its efficacy in postoperative settings remains limited. This prospective, randomized controlled trial aims to provide high-quality data on the role of KinesioTaping as a non-pharmacological adjunct for pain management in patients undergoing cardiac surgery.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for phase_2

Timeline
Completed

Started Aug 2025

Shorter than P25 for phase_2

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 20, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

August 1, 2025

Completed
14 days until next milestone

Study Start

First participant enrolled

August 15, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 12, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 12, 2025

Completed
Last Updated

December 19, 2025

Status Verified

December 1, 2025

Enrollment Period

4 months

First QC Date

July 20, 2025

Last Update Submit

December 14, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Day 3 Visual Analogue Scale Pain Score

    Visual analog scale pain score on the 3th day after cardiac surgery. Pain is defined as no pain (0) or unbearable pain (10). 0 = No pain, 1-3 = Mild pain, 4-6 = Moderate pain, 7-10 = Severe pain

    3 day

Study Arms (2)

Kinesiotaping group

EXPERIMENTAL

In this group, KinesioTaping will be applied alongside routine pain management.

Other: Kinesiotaping

Routine treatment group

ACTIVE COMPARATOR

This group will be managed with standard hospital-based painkiller administration.

Drug: Dexketoprofen, tramadol

Interventions

In this group, KinesioTaping will be applied around the thoracic drain sites alongside standard analgesic therapy. This physical therapy technique uses elastic tapes placed on the skin to support healing, reduce pain, and improve patient comfort. The tapes will remain in place for 2-3 days and will be removed together with the drains.

Also known as: Kinesiotape
Kinesiotaping group

Patients in this group will be treated with painkillers consisting of tramadol and dexketoprofen.

Routine treatment group

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Elective cardiac surgery cases
  • Patients who are stable until the removal of the chest drain
  • Patients who do not experience serious complications such as bleeding or neurological problems

You may not qualify if:

  • Patients undergoing emergency cardiac surgery,
  • Patients with early post-cardiac surgery mortality,
  • Patients with conditions requiring reoperation, such as bleeding,
  • Patients for whom a pain score cannot be measured, such as neurological complications

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kastamonu Education and Research Hospital

Kastamonu, Kastamonu, 37200, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Athletic Tapetramadol, dexketoprofen drug combination

Intervention Hierarchy (Ancestors)

BandagesEquipment and SuppliesOrthotic DevicesOrthopedic EquipmentSurgical Equipment

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor Literally: Doctor Teaching Member

Study Record Dates

First Submitted

July 20, 2025

First Posted

August 1, 2025

Study Start

August 15, 2025

Primary Completion

December 12, 2025

Study Completion

December 12, 2025

Last Updated

December 19, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will share

yes

Time Frame
Data will become available persistantly on 2.2.2026.
Access Criteria
Upon reasonable request principal investigator will share the data.

Locations