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The Effect of Kinesio Tape on Pain Management in Laparoscopic Gynecological Surgeries.

The Effect of Kinesio Tape on Pain Management in Laparoscopic Gynecological Surgeries: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06648811
Enrollment
54
Registered
2024-10-18
Start date
2024-10-15
Completion date
2025-02-01
Last updated
2025-10-22

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

Conditions

Gynecological Laparoscopy

Brief summary

Kinesio tapes have been used in medicine to reduce pain in various situations. It is an easy applicable and effective tape. The possible affect of this tape will be assessed in patients undergoing gynecological laparoscopic surgeries.

Detailed description

Kinesio tape is frequently used for pain palliation in medicine including orthopedics, physical therapy and rehabilitation, and dentistry. Recent studies show that it alleviates the amount of postoperative perceived pain in obstetrics and general surgery. In our study, we plan to contribute to the medical literature by studying its effect on pain palliation in patients undergoing laparoscopic gynecological surgery.

Interventions

Kinesio tapes will be applied to the patients in the study group after gynecological laparoscopic operations. The routine pain management will also be provided in these patients in addition to the kinesio tapes. Only postoperative pain management will be provided to the patients in the control group. The patients will be consisted of only the patients who will be operated laparoscopically for gynecological diseases.

Sponsors

Mersin University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* being older than 18 years old female gender benign gynecologic conditions patients who underwent laparoscopic surgery patients who do not have any predisposing factors that aggreviate pain no history of malignancy no prior abdominal surgery patients who do not regularly take antiinflammatory medication patients who give permission to participate

Exclusion criteria

* being younger than 18 years old non-female gender having malignancies patients who underwent laparatomy patients with predisposing factors that aggrevate pain having prior abdominal surgery patients taking regular antiinflammatory medications who do not want to participate

Design outcomes

Primary

MeasureTime frameDescription
Amount of perceived pain36 hours from the operationThe amount of postoperative pain will be measured by using visual analogue scales (score ranges from 0 to 100 mm, higher scores indicate more pain)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026