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Clinical Trials/NCT06485011
NCT06485011
Completed
Not Applicable

Comparison Of Outcome Of Wound Closure After Thyroid Surgery With And Without Platysma Suturing

Children Hospital and Institute of Child Health, Lahore1 site in 1 country72 target enrollmentJanuary 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Acute Postoperative
Sponsor
Children Hospital and Institute of Child Health, Lahore
Enrollment
72
Locations
1
Primary Endpoint
Post operative Pain
Status
Completed
Last Updated
last year

Overview

Brief Summary

Comparison Of Outcome Of Wound Closure After Thyroid Surgery With And Without Platysma Suturing in terms of wound scar and pain.

Detailed Description

This randomized controlled trail was conducted at Surgical Ward from January 2021 to July 2021. Materials and Methods Total 72 patients (indicated for thyroid surgery) who were fulfilling the inclusion criteria were enrolled. Patients were divided randomly into two groups by using lottery method. In Group A patients wound closure was done without Platysma Suturing and in Group-B patients wound closure was done with Platysma Suturing. Pain assessment was done with the help of VAS after surgery (6, Hours, 24 hours, 48 hours). Scar assessment was carried out with the help of POSAS. All this information was noted by the researcher himself and noted on a well-designed questionnaire.

Registry
clinicaltrials.gov
Start Date
January 1, 2021
End Date
September 1, 2021
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Children Hospital and Institute of Child Health, Lahore
Responsible Party
Principal Investigator
Principal Investigator

Muhammad Adeel Ashiq

Principal Investigator

Children Hospital and Institute of Child Health, Lahore

Eligibility Criteria

Inclusion Criteria

  • : Both men and women patients in the age range (20-70 years) undergoing primary thyroid surgery were included.

Exclusion Criteria

  • Patients with disorders of wound healing, diabetes mellitus, Pre-operative known malignant condition, history of neck surgery or not willing to participate in the study were excluded.

Outcomes

Primary Outcomes

Post operative Pain

Time Frame: 48 hours

Pain assessed on visual analogue scale. higher the VAS score means more pain and lower score mean less pain

Study Sites (1)

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