Postoperative PainNCT06910215
Effect of Elastic Therapeutic Taping on Post-Sternotomy Pain in Coronary Artery Bypass Graft Surgery
A study testing Elastic therapeutic taping and Therapeutic Taping on Non-Surgical Areas in people with Postoperative Pain and Sternotomy, run by Abant Izzet Baysal University at 1 site in Turkey (Türkiye).
Trial summary
This research study aims to find out whether elastic therapeutic taping can help reduce pain after heart surgery, specifically coronary artery bypass grafting (CABG), which is done using a surgical cut through the breastbone (sternotomy). Read more about this study
- Who is it for?
- Ages 18 to 75 years
- Conditions the study is for
- Postoperative Pain, Sternotomy, Pain Management
- What is being tested?
- Elastic therapeutic taping and Therapeutic Taping on Non-Surgical Areas
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 195 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 22 Jan 2025to 24 Dec 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age between 18 and 75 years
- Undergoing elective coronary artery bypass graft (CABG) surgery via sternotomy
- Able to understand and communicate effectively
- Willing to provide informed consent
Who cannot join
- Presence of dermatological conditions or open wounds in the sternotomy area
- History of allergy to elastic therapeutic tape or adhesive materials
- Diagnosis of neurological or psychiatric conditions that may affect pain perception
- Currently taking medications that significantly alter pain sensitivity (e.g., neuropathic pain medications)
- Participation in another interventional clinical study within the past 30 days
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Bolu Abant Izzet Baysal University
Bolu, Bolu, 14030
About this study
Official title: The Effectiveness of Elastic Therapeutic Taping in Pain Management After Sternotomy: A Randomized Controlled Double-Blind Study in Patients Undergoing Coronary Artery Bypass Grafting Surgery
This research study aims to find out whether elastic therapeutic taping can help reduce pain after heart surgery, specifically coronary artery bypass grafting (CABG), which is done using a surgical cut through the breastbone (sternotomy). This type of surgery often causes pain that makes it hard for patients to breathe deeply, move around, or recover quickly. Managing this pain in a safe and effective way is important for better healing and quality of life.
Elastic therapeutic taping is a method where special stretchy tape is applied to the skin to reduce pain and support the muscles. It is already used for other conditions like back or shoulder pain. In this study, researchers want to see if this taping method can also help people recover better after heart surgery by lowering pain, helping movement, and improving sleep and emotional well-being.
Read more
A total of 195 participants who had planned (elective) CABG surgery will be included in the study. People will be placed into one of three groups:
One group will get real elastic tape applied near the surgical area.
One group will get fake (placebo) tape that looks the same but has no medical effect.
One group will get a different kind of supportive treatment in other body areas.
Neither the patients nor the people measuring the results will know which group each person is in. This is called a "double-blind randomized controlled trial," which is the best way to get reliable results.
The researchers will check each participant's pain levels using a visual scale, and will also look at other things like oxygen levels, sleep quality, anxiety, how well they move, and how much pain medicine they use. These checks will happen several times in the first two days after surgery.
The taping is safe and non-invasive. Some people may experience mild skin irritation, but no serious side effects are expected. Participation is voluntary, and people can leave the study at any time. No payments will be made to participants, and all medical services related to the study will be free of charge.
This study is supported by Bolu Abant Izzet Baysal University. The results may help offer a new, drug-free option for managing pain after heart surgery and may improve patients' recovery experience.
Read the detailed description
This randomized, controlled, double-blind clinical trial is designed to assess the efficacy of elastic therapeutic taping in reducing post-sternotomy pain in patients undergoing elective coronary artery bypass grafting (CABG) via median sternotomy. The study will be conducted at a single tertiary care center and will enroll 195 participants aged 18-75 years.
Participants will be randomized into three equal groups (n = 65 per group) using a computer-generated block randomization method. Allocation concealment will be maintained using sealed opaque envelopes. The interventions will be applied within 6-8 hours after extubation in the intensive care unit, and participants will be followed for 48 hours post-intervention.
Intervention Details:
Elastic Therapeutic Taping Group: Kinesio tape will be applied bilaterally, approximately 3 cm lateral to the sternotomy incision. The tape will be applied using standardized protocols with 25-35% stretch, following the muscle facilitation technique for pain relief and proprioceptive input.
Placebo Taping Group: Identical tape will be applied in the same locations, but without any stretch, and without following therapeutic taping principles. This group controls for the tactile and visual stimulus of taping.
Sham Taping (Contextual Support) Group: Tape will be applied to non-surgical, compensatory areas (e.g., shoulders, paravertebral region, or intercostal muscles) using a standard method, but in locations unrelated to the surgical site. This group is intended to control for the psychological and contextual effects of physical touch and therapist interaction.
All taping procedures will be performed by certified kinesio taping practitioners. The tape will remain in place for 48 hours unless early removal is required due to adverse skin reactions.
Blinding:
The study employs a double-blind design. Participants, outcome assessors, and data analysts will be blinded to group allocation. Intervention providers will not be involved in outcome assessment or data analysis.
Data Collection and Monitoring:
Primary and secondary outcome data will be collected at baseline (prior to intervention), and at 12, 24, and 48 hours post-intervention. Adherence to the intervention and any adverse events (e.g., skin irritation, allergic reaction) will be recorded. A dedicated safety officer will monitor for protocol adherence and unexpected complications.
Statistical Plan:
All analyses will follow an intention-to-treat approach. Descriptive statistics will summarize baseline characteristics. Normality will be assessed using the Shapiro-Wilk test. Between-group differences at each time point will be analyzed using one-way ANOVA or Kruskal-Wallis test. Repeated measures ANOVA or Friedman test will be used for within-group temporal comparisons. Bonferroni correction will adjust for multiple comparisons. Effect sizes (Cohen's d, partial eta squared) will be calculated.
Ethical Considerations:
The study protocol has been approved by the relevant institutional ethics committee. Written informed consent will be obtained from all participants. No experimental drugs or devices will be used. The tape used is CE-certified for medical use. The study adheres to the principles of the Declaration of Helsinki and Good Clinical Practice guidelines.
This study aims to provide high-quality evidence on the effectiveness of elastic therapeutic taping as a non-pharmacological intervention for managing early postoperative pain and improving recovery outcomes in CABG patients.
- Being tested
- Elastic therapeutic taping, Placebo Elastic Therapeutic Taping, Therapeutic Taping on Non-Surgical Areas
- Keywords
- Postoperative Pain, Sternotomy, Kinesio Tape, Anxiety, Sleep Quality, Coronary Artery Bypass
- Medical subject headings
- Pain, Postoperative, Agnosia, Anxiety Disorders, Sleep Initiation and Maintenance Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Elastic therapeutic tapingOther
Elastic therapeutic taping is a non-invasive method that uses a specially designed elastic cotton tape applied directly to the skin. In this study, it is used to support pain management after open-heart surgery (CABG via sternotomy). The tape is applied near the surgical site to gently lift the skin, which may help reduce pain, improve circulation, and support healing. The application is done by a trained physiotherapist following a standardized taping protocol. The tape remains on the skin for up to 48 hours.
Placebo Elastic Therapeutic TapingOther
In this group, the same type of elastic tape used in the therapeutic group is applied to the skin near the surgical area, but without any stretch or therapeutic technique. The tape does not provide physical support or intended therapeutic effects. It is used to help researchers understand whether any improvements are due to the taping itself or simply from receiving an intervention. The tape remains in place for up to 48 hours and is applied by trained personnel using a standardized, non-therapeutic method.
Therapeutic Taping on Non-Surgical AreasOther
In this group, elastic therapeutic tape is applied to body areas not directly related to the surgery, such as the shoulder, back, or rib area. The purpose is not to treat pain at the surgical site, but to simulate the experience of receiving a physical intervention. This approach helps researchers understand the potential impact of attention, expectation, or psychological support related to being part of a study. The tape is applied gently without therapeutic intent and stays on for up to 48 hours
| Study group | Role | What they receive |
|---|---|---|
| Elastic Therapeutic Taping Group | Experimental | Participants in this group will receive elastic therapeutic taping (kinesio taping) applied bilaterally 3 cm lateral to the sternotomy incision site. The tape will be applied with standardized tension and technique by a trained physiotherapist within 24 hours post-CABG surgery. The tape will remain in place for 48 hours. The goal is to assess the therapeutic effect of kinesio taping on postoperative pain and related outcomes. Receives: Other: Elastic therapeutic taping |
| Placebo Taping Group | Placebo comparator | Participants in this group will receive placebo taping to the same area (3 cm lateral to the sternotomy incision), using the same type of tape but without any tension or therapeutic intent. The tape will be applied by the same trained team, in an identical manner visually, but with no mechanical stretch. The tape will also remain in place for 48 hours. This will help control for the placebo effect of the taping procedure. Receives: Other: Placebo Elastic Therapeutic Taping |
| Psychosocial Support Group | Sham comparator | Participants in this group will receive elastic therapeutic tape applied to unrelated regions of the body (e.g., shoulder, back, or intercostal muscles) not associated with the surgical area. The purpose is to account for contextual or psychosocial effects of receiving an intervention. The tape will be applied without therapeutic intent for the surgical pain, and will stay in place for 48 hours. Receives: Other: Therapeutic Taping on Non-Surgical Areas |
What is being measured
The primary outcome is the main question the study is designed to answer.
Pain Intensity (Visual Analog Scale - VAS)
Change in pain intensity will be assessed using the Visual Analog Scale (VAS), a 100 mm horizontal line where participants rate their pain from 0 (no pain) to 100 (worst imaginable pain).
Measured: Baseline, 12 hours, 24 hours, and 48 hours after intervention
Secondary outcomes (9)
Oxygen Saturation (SpO₂)
Peripheral oxygen saturation measured using a pulse oximeter to assess potential respiratory improvement.
Measured: Baseline, 12 hours, 24 hours, and 48 hours after intervention
Sleep Quality (VAS)
Participants will rate their sleep quality using a Visual Analog Scale (0 = very poor, 100 = excellent).
Measured: Baseline, 24 hours, and 48 hours after intervention
Anxiety Level (VAS)
Participants will rate their anxiety level using a Visual Analog Scale (0 = no anxiety, 100 = extreme anxiety).
Measured: Baseline, 12 hours, 24 hours, and 48 hours post-intervention
Functional Mobility (Timed Up and Go Test)
Time (in seconds) taken by participants to rise from a chair, walk 3 meters, turn around, walk back, and sit down.
Measured: Baseline, 12 hours, 24 hours, and 48 hours after intervention
Analgesic Use
Total dosage of analgesic medication used during the first 48 hours post-surgery.
Measured: 0-48 hours post-intervention
Length of Hospital Stay
Number of days from the date of surgery to the date of hospital discharge, as documented in the patient's medical record.
Measured: From the date of surgery until hospital discharge, assessed up to 30 days postoperatively.
Fatigue Severity (VAS)
Participants will rate their level of fatigue on a 100 mm Visual Analog Scale, where 0 indicates "no fatigue" and 100 indicates "extreme fatigue."
Measured: Baseline,12 hours, 24 hours, and 48 hours post-intervention
Pain Intensity While Coughing (VAS)
Pain experienced during coughing will be measured using a 100 mm Visual Analog Scale, where 0 represents "no pain" and 100 represents "worst possible pain."
Measured: Baseline, 12 hours, 24 hours, and 48 hours post-intervention
Pain Intensity at Rest (VAS)
Participants will rate their resting pain intensity using a 100 mm Visual Analog Scale (VAS), where 0 is "no pain" and 100 is "worst pain imaginable."
Measured: Baseline, 12 hours, 24 hours, and 48 hours post-intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Apr 2025
- Study start22 Jan 2025
- Primary completion24 Dec 2025
- Study completion24 Dec 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Postoperative PainStudies of the same condition, open and under way.
- More trials run by Abant Izzet Baysal UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 195 participants (actual)
Sponsor and investigators
- Lead sponsor
- Abant Izzet Baysal University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Alp Ozel, Abant Izzet Baysal University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06910215
- Sponsor's protocol ID
- AIBU-FTR-AO-03
- Status last verified
- Dec 2025
- First submitted
- 25 Mar 2025
- Last updated
- 31 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Individual participant data (de-identified) that underlie the results reported in this study will be made available upon reasonable request from qualified researchers, following publication. Data will be shared through institutional approval processes in accordance with ethical guidelines.
Publications
Ozel A, Ugras UA, Uysal MF, Ucaroglu ER. Effectiveness of elastic therapeutic taping in pain management after median sternotomy: A randomized controlled trial. PLoS One. 2026 Sep 28;21(9):e0359282. doi: 10.1371/journal.pone.0359282. eCollection 2026.
PubMed 42804437
Study at a glance
From the registry record, last updated by the sponsor on 31 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effectiveness of Elastic Therapeutic Taping in Pain Management After Sternotomy: A Randomized Controlled Double-Blind Study in Patients Undergoing Coronary Artery Bypass Grafting Surgery
- ClinicalTrials.gov ID
- NCT06910215
- Acronym / sponsor ID
- AIBU-FTR-AO-03
- Keywords
- Postoperative Pain, Sternotomy, Kinesio Tape, Anxiety, Sleep Quality, Coronary Artery Bypass
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 195 participants (actual)
- Lead sponsor
- Abant Izzet Baysal UniversityUniversity, hospital or other
- Study start
- 22 Jan 2025 (actual)
- Primary completion
- 24 Dec 2025 (actual)
- Study completion
- 24 Dec 2025 (actual)
- First posted
- 4 Apr 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This research study aims to find out whether elastic therapeutic taping can help reduce pain after heart surgery, specifically coronary artery bypass grafting (CABG), which is done using a surgical cut through the breastbone (sternotomy). This type of surgery often causes pain that makes it hard for patients to breathe deeply, move around, or recover quickly. Managing this pain in a safe and effective way is important for better healing and quality of life.
Elastic therapeutic taping is a method where special stretchy tape is applied to the skin to reduce pain and support the muscles. It is already used for other conditions like back or shoulder pain. In this study, researchers want to see if this taping method can also help people recover better after heart surgery by lowering pain, helping movement, and improving sleep and emotional well-being.
A total of 195 participants who had planned (elective) CABG surgery will be included in the study. People will be placed into one of three groups:
One group will get real elastic tape applied near the surgical area.
One group will get fake (placebo) tape that looks the same but has no medical effect.
One group will get a different kind of supportive treatment in other body areas.
Neither the patients nor the people measuring the results will know which group each person is in. This is called a "double-blind randomized controlled trial," which is the best way to get reliable results.
The researchers will check each participant's pain levels using a visual scale, and will also look at other things like oxygen levels, sleep quality, anxiety, how well they move, and how much pain medicine they use. These checks will happen several times in the first two days after surgery.
The taping is safe and non-invasive. Some people may experience mild skin irritation, but no serious side effects are expected. Participation is voluntary, and people can leave the study at any time. No payments will be made to participants, and all medical services related to the study will be free of charge.
This study is supported by Bolu Abant Izzet Baysal University. The results may help offer a new, drug-free option for managing pain after heart surgery and may improve patients' recovery experience.
Detailed description
This randomized, controlled, double-blind clinical trial is designed to assess the efficacy of elastic therapeutic taping in reducing post-sternotomy pain in patients undergoing elective coronary artery bypass grafting (CABG) via median sternotomy. The study will be conducted at a single tertiary care center and will enroll 195 participants aged 18-75 years.
Participants will be randomized into three equal groups (n = 65 per group) using a computer-generated block randomization method. Allocation concealment will be maintained using sealed opaque envelopes. The interventions will be applied within 6-8 hours after extubation in the intensive care unit, and participants will be followed for 48 hours post-intervention.
Intervention Details:
Elastic Therapeutic Taping Group: Kinesio tape will be applied bilaterally, approximately 3 cm lateral to the sternotomy incision. The tape will be applied using standardized protocols with 25-35% stretch, following the muscle facilitation technique for pain relief and proprioceptive input.
Placebo Taping Group: Identical tape will be applied in the same locations, but without any stretch, and without following therapeutic taping principles. This group controls for the tactile and visual stimulus of taping.
Sham Taping (Contextual Support) Group: Tape will be applied to non-surgical, compensatory areas (e.g., shoulders, paravertebral region, or intercostal muscles) using a standard method, but in locations unrelated to the surgical site. This group is intended to control for the psychological and contextual effects of physical touch and therapist interaction.
All taping procedures will be performed by certified kinesio taping practitioners. The tape will remain in place for 48 hours unless early removal is required due to adverse skin reactions.
Blinding:
The study employs a double-blind design. Participants, outcome assessors, and data analysts will be blinded to group allocation. Intervention providers will not be involved in outcome assessment or data analysis.
Data Collection and Monitoring:
Primary and secondary outcome data will be collected at baseline (prior to intervention), and at 12, 24, and 48 hours post-intervention. Adherence to the intervention and any adverse events (e.g., skin irritation, allergic reaction) will be recorded. A dedicated safety officer will monitor for protocol adherence and unexpected complications.
Statistical Plan:
All analyses will follow an intention-to-treat approach. Descriptive statistics will summarize baseline characteristics. Normality will be assessed using the Shapiro-Wilk test. Between-group differences at each time point will be analyzed using one-way ANOVA or Kruskal-Wallis test. Repeated measures ANOVA or Friedman test will be used for within-group temporal comparisons. Bonferroni correction will adjust for multiple comparisons. Effect sizes (Cohen's d, partial eta squared) will be calculated.
Ethical Considerations:
The study protocol has been approved by the relevant institutional ethics committee. Written informed consent will be obtained from all participants. No experimental drugs or devices will be used. The tape used is CE-certified for medical use. The study adheres to the principles of the Declaration of Helsinki and Good Clinical Practice guidelines.
This study aims to provide high-quality evidence on the effectiveness of elastic therapeutic taping as a non-pharmacological intervention for managing early postoperative pain and improving recovery outcomes in CABG patients.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Elastic Therapeutic Taping Group | Experimental | Other: Elastic therapeutic tapingParticipants in this group will receive elastic therapeutic taping (kinesio taping) applied bilaterally 3 cm lateral to the sternotomy incision site. The tape will be applied with standardized tension and technique by a trained physiotherapist within 24 hours post-CABG surgery. The tape will remain in place for 48 hours. The goal is to assess the therapeutic effect of kinesio taping on postoperative pain and related outcomes. |
| Placebo Taping Group | Placebo comparator | Other: Placebo Elastic Therapeutic TapingParticipants in this group will receive placebo taping to the same area (3 cm lateral to the sternotomy incision), using the same type of tape but without any tension or therapeutic intent. The tape will be applied by the same trained team, in an identical manner visually, but with no mechanical stretch. The tape will also remain in place for 48 hours. This will help control for the placebo effect of the taping procedure. |
| Psychosocial Support Group | Sham comparator | Other: Therapeutic Taping on Non-Surgical AreasParticipants in this group will receive elastic therapeutic tape applied to unrelated regions of the body (e.g., shoulder, back, or intercostal muscles) not associated with the surgical area. The purpose is to account for contextual or psychosocial effects of receiving an intervention. The tape will be applied without therapeutic intent for the surgical pain, and will stay in place for 48 hours. |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Age between 18 and 75 years
- Undergoing elective coronary artery bypass graft (CABG) surgery via sternotomy
- Able to understand and communicate effectively
- Willing to provide informed consent
Key exclusion criteria (5 listed)
- Presence of dermatological conditions or open wounds in the sternotomy area
- History of allergy to elastic therapeutic tape or adhesive materials
- Diagnosis of neurological or psychiatric conditions that may affect pain perception
- Currently taking medications that significantly alter pain sensitivity (e.g., neuropathic pain medications)
- Participation in another interventional clinical study within the past 30 days
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Elastic therapeutic tapingElastic therapeutic taping is a non-invasive method that uses a specially designed elastic cotton tape applied directly to the skin. In this study, it is used to support pain management after open-heart surgery (CABG via sternotomy). The tape is applied near the surgical site to gently lift the skin, which may help reduce pain, improve circulation, and support healing. The application is done by a trained physiotherapist following a standardized taping protocol. The tape remains on the skin for up to 48 hours. | Other | Elastic Therapeutic Taping Group |
| Placebo Elastic Therapeutic TapingIn this group, the same type of elastic tape used in the therapeutic group is applied to the skin near the surgical area, but without any stretch or therapeutic technique. The tape does not provide physical support or intended therapeutic effects. It is used to help researchers understand whether any improvements are due to the taping itself or simply from receiving an intervention. The tape remains in place for up to 48 hours and is applied by trained personnel using a standardized, non-therapeutic method. | Other | Placebo Taping Group |
| Therapeutic Taping on Non-Surgical AreasIn this group, elastic therapeutic tape is applied to body areas not directly related to the surgery, such as the shoulder, back, or rib area. The purpose is not to treat pain at the surgical site, but to simulate the experience of receiving a physical intervention. This approach helps researchers understand the potential impact of attention, expectation, or psychological support related to being part of a study. The tape is applied gently without therapeutic intent and stays on for up to 48 hours | Other | Psychosocial Support Group |
Primary outcome
Pain Intensity (Visual Analog Scale - VAS)
Time frame: Baseline, 12 hours, 24 hours, and 48 hours after intervention
Change in pain intensity will be assessed using the Visual Analog Scale (VAS), a 100 mm horizontal line where participants rate their pain from 0 (no pain) to 100 (worst imaginable pain).
9 secondary outcomes
Oxygen Saturation (SpO₂)
Time frame: Baseline, 12 hours, 24 hours, and 48 hours after intervention
Sleep Quality (VAS)
Time frame: Baseline, 24 hours, and 48 hours after intervention
Anxiety Level (VAS)
Time frame: Baseline, 12 hours, 24 hours, and 48 hours post-intervention
Functional Mobility (Timed Up and Go Test)
Time frame: Baseline, 12 hours, 24 hours, and 48 hours after intervention
Analgesic Use
Time frame: 0-48 hours post-intervention
Length of Hospital Stay
Time frame: From the date of surgery until hospital discharge, assessed up to 30 days postoperatively.
Fatigue Severity (VAS)
Time frame: Baseline,12 hours, 24 hours, and 48 hours post-intervention
Pain Intensity While Coughing (VAS)
Time frame: Baseline, 12 hours, 24 hours, and 48 hours post-intervention
Pain Intensity at Rest (VAS)
Time frame: Baseline, 12 hours, 24 hours, and 48 hours post-intervention
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Dec 2025.
- Derived from this study: PubMed 42804437Ozel A, Ugras UA, Uysal MF, Ucaroglu ER. Effectiveness of elastic therapeutic taping in pain management after median sternotomy: A randomized controlled trial. PLoS One. 2026 Sep 28;21(9):e0359282. doi: 10.1371/journal.pone.0359282. eCollection 2026.
- Individual participant dataSharing planned: Yes. Individual participant data (de-identified) that underlie the results reported in this study will be made available upon reasonable request from qualified researchers, following publication. Data will be shared through institutional approval processes in accordance with ethical guidelines.
Related trials for Postoperative Pain
RecruitingPhase 4
ESP Blocks for Posterior Spinal Fusion
Postoperative Pain
Recruiting
Effect of Cryotherapeutic and Nanotherapeutic Sodium Hypochlorite on Post-Operative Endodontic Pain.
Symptomatic Irreversible Pulpitis, Symptomatic Apical Periodontitis
RecruitingPhase 2
REctus Sheath Trial
Acute Pain, Postoperative Pain, Acute
Not yet recruiting
Effect of Pectoral Nerve Block (PECS) Using Magnesium Sulfate Added to Dexamethasone on Quality of Recovery and Chronic Post-Mastectomy Pain
Breast Cancer, Postoperative Pain
Active, not recruitingPhase 4
Effect of Dexmedetomidine on Postoperative Pain in Spinal Anesthesia for Cesarean Section at Assuit University Hospital
Cesarean Section
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Elastic therapeutic taping and Therapeutic Taping on Non-Surgical Areas in people with Postoperative Pain and Sternotomy, run by Abant Izzet Baysal University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 31 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Pain Intensity (Visual Analog Scale - VAS) (time frame: Baseline, 12 hours, 24 hours, and 48 hours after intervention). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06910215, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Dec 2025.