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CompletedNCT07098962KT-DrainUpdated Jun 9, 2026

KinesioTaping for Thoracic Drain Support

A Phase 2/3 interventional study of Kinesiotaping and paracetamol tramadol in Primary Condition: Pain, Postoperative and Associated Conditions: Cardiac Surgical Procedures, Thoracic Surgery, sponsored by Kastamonu University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2026-06-09.

Sponsored by Kastamonu University · Phase 2/3, Interventional, and Supportive care

Phase
Phase 2/3
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years to 100 Years
Sex
All
01

Study 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.

Read the detailed description

Postoperative pain following cardiac surgery is a significant clinical concern that can hinder early mobilization, reduce patient satisfaction, prolong hospital stay, and increase the risk of respiratory complications such as atelectasis and pneumonia. While pharmacological analgesia remains the mainstay of treatment, non-pharmacological adjuncts are increasingly being explored to enhance pain control and reduce reliance on opioids.

KinesioTaping (KT), a method originally developed for musculoskeletal conditions, involves the application of elastic therapeutic tape to the skin with the aim of supporting soft tissue structures, enhancing lymphatic and blood flow, and modulating nociceptive input via stimulation of cutaneous mechanoreceptors. In the context of postoperative care, KT may also help reduce localized edema, support incision sites, and promote a sense of physical stability that contributes to pain relief.

Despite its growing popularity in rehabilitation and sports medicine, the use of KinesioTaping in postoperative settings-particularly in cardiothoracic surgery-remains under-investigated. Limited studies have suggested potential benefits in reducing pain and improving functional outcomes, but current evidence is inconclusive and often methodologically limited.

This prospective, randomized controlled trial aims to evaluate the effectiveness of KinesioTaping when applied around mediastinal and thoracic drain sites in patients undergoing cardiac surgery. The primary objective is to assess postoperative pain levels using validated pain scales (e.g., VAS) in patients receiving KT versus those receiving standard care without taping. Secondary outcomes include opioid consumption, time to ambulation, respiratory function (spirometry or incentive spirometry use), incidence of atelectasis, and patient satisfaction scores.

By providing high-quality evidence on a low-cost, non-invasive, and easily applicable intervention, this study seeks to clarify the potential role of KinesioTaping as an adjunctive tool in postoperative pain management protocols following cardiac surgery.

02

Conditions studied

  • Primary Condition: Pain, Postoperative
  • Associated Conditions: Cardiac Surgical Procedures, Thoracic Surgery
03

In context

Lead sponsor

Kastamonu University is the lead sponsor of 46 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 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

Exclusion criteria

Exclusion Criteria:

  • 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
05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
100 participants (actual)

Study arms

  • Experimental
    Kinesiotaping group

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

    Other: Kinesiotaping

  • Active comparator
    Routine treatment group

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

    Drug: paracetamol tramadol

Interventions

  • OtherKinesiotaping

    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

  • Drugparacetamol tramadol

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

    Also known as: paracetamol, tramadol

06

What researchers measure

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

    Time frame: 3 day

07

Study locations

1 site
  • Kastamonu Education and Research Hospital
    Kastamonu, Kastamonu 37200, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Yes — yes

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07098962
Lead sponsor
Kastamonu University
Responsible party
İsmail DAL (Assistant Professor Literally: Doctor Teaching Member, Kastamonu University) — Principal investigator
First posted
Aug 1, 2025
Start date
Aug 15, 2025
Primary completion
Dec 12, 2025
Completion
Dec 12, 2025
Last update
Jun 9, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

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