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NCT04937114 Clinical Trial

Unidirectional Barbed Sutures in Mucogingival Procedures

Wound Heal Clinical Trial

Official title:
Efficacy of Unidirectional Barbed Sutures on Various Outcomes in Mucogingival Procedures

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04937114
Other study ID # SVSIDS/PERIO/5/2020
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 2021
Est. completion date December 2022

Study information
Verified date June 2021
Source SVS Institute of Dental Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to compare the efficacy of barbed suture with conventional suture in muco-gingival surgeries.

Description:

Experimental: Main treatment group, flap will be approximated using conventional, simple continuous suturing with barbed sutures. Comparator: In patients allocated to control group, flap will be approximated using conventional, simple continuous suturing with conventional sutures.

Recruitment information / eligibility
Status Recruiting
Enrollment 12
Est. completion date December 2022
Est. primary completion date December 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - Systemically healthy individuals within an age group of 20-50yrs with presence of attached gingiva, shallow vestibule and frenum interfering with the marginal gingiva. Exclusion Criteria: - Medically compromised patients. - Subjects who underwent radiotherapy or chemotherapy in the past 12 months. - Smokers

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Barbed suture
Experimental: Wound will be closed using unidirectional barbed sutures in muco-gingival surgeries Active Comparator: Wound will be closed using conventional sutures in muco-gingival surgeries

Locations
Country Name City State
India SVS Institute of Dental Sciences, Mahabubnagar Hyderabad Telangana

Sponsors (1)
Lead Sponsor Collaborator
SVS Institute of Dental Sciences

Country where clinical trial is conducted

India, 

Outcome
Type Measure Description Time frame Safety issue
Primary To assess primary wound closure Primary wound closure and early wound healing by EHS at 7days,14days,21days Baseline to 21days
Secondary To assess pain Pain by Visual Analogous Scale immediately Baseline to 21days
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