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CompletedNCT06485011Updated Jul 3, 2024

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

An interventional study of Paltysma suturing and Without Platysma suturing in Pain, Acute Postoperative, sponsored by Children Hospital and Institute of Child Health, Lahore. Completed at 1 site in Pakistan. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-07-03.

Sponsored by Children Hospital and Institute of Child Health, Lahore · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 years 5 months after the study started (first participant enrolled Jan 2021, registered Jun 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
72
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

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

Read the 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.

02

Conditions studied

  • Pain, Acute Postoperative

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Keywords

  • Thyroid surgery
  • scar
  • visual analog scale
03

In context

Pain, Postoperative

5,093 studies on the registry are indexed under Pain, Postoperative; 1,140 are open to participants now.

This study's enrollment of 72 is close to the median of 75 across 4,344 interventional studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Children Hospital and Institute of Child Health, Lahore is the lead sponsor of 9 studies on the registry; 2 are open to participants now.

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

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Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

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.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
72 participants (actual)

Study arms

  • Experimental
    With Platysma suturing

    platysma muscle was sutured in this group

    Procedure: Paltysma suturing

  • Experimental
    Without Platysma suturing

    platysma muscle was not sutured in this group

    Procedure: Without Platysma suturing

Interventions

  • ProcedurePaltysma suturing

    platysma muscle was sutured in this group with vicryl

  • ProcedureWithout Platysma suturing

    platysma muscle was not sutured in this group

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What researchers measure

Primary outcomes

  1. Post operative Pain

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

    Time frame: 48 hours

07

Study locations

1 site
  • The Children Hospital
    Lahore, Punjab 42000, Pakistan
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References and documents

Individual participant data

Plan to share: No — No plan of sharing

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 Jul 3, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06485011
Lead sponsor
Children Hospital and Institute of Child Health, Lahore
Responsible party
Muhammad Adeel Ashiq (Principal Investigator, Children Hospital and Institute of Child Health, Lahore) — Principal investigator
First posted
Jul 3, 2024
Start date
Jan 1, 2021
Primary completion
Jul 1, 2021
Completion
Sep 1, 2021
Last update
Jul 3, 2024

Study contacts

Adeel Ashiq, MS
principal investigator · The Children Hospital

Oversight

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

Not currently enrolling

This study is completed, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

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