Effect of Two Methods of Soft Tissue Augmentation for Socket Closure on Soft Tissue Landmarks and Ridge Dimensions

Recession, Gingival Clinical Trial

Official title:

"Effect of Two Methods of Soft Tissue Augmentation for Socket Closure on Soft Tissue Landmarks and Ridge Dimensions- Results From Software-based Analysis of Clinical Data"

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05342649
• Other study ID #: SVSIDS/PERIO/1/2017
• Status: Completed
• Phase: N/A
• Start date: January 1, 2018
• Est. completion date: June 20, 2019

Study information

• Verified date: April 2022
• Source: SVS Institute of Dental Sciences
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To evaluate the effect of Connective Tissue Graft and Pediculated-Connective Tissue Graft for extraction socket closure on soft tissue landmarks and ridge dimensions.

Description:

45 subjects were randomized into two groups Experimental: Main treatment group P-CTG group Active Comparator: Control group CTG group.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 45
• Est. completion date: June 20, 2019
• Est. primary completion date: May 1, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 35 Years to 45 Years

Eligibility

Inclusion Criteria:

• Based on the Extraction Defect Sounding(EDS) Classification given by Caplanis et al,

1. Systemically healthy subjects within the age group of 20-50years

2. with extraction defect type 2 and type 3 were included in this study

Exclusion Criteria:

1. Medically compromised patients

2. Subjects who underwent radiotherapy or chemotherapy and

3. Smokers

Related Conditions & MeSH terms

• Gingival Recession
• Recession, Gingival

Intervention

Procedure:
• P-CTG
soft tissue closure of extraction sockets was done by pediculated connective tissue grafts (P-CTG)
• CTG
soft tissue closure of extraction sockets was done by connective tissue grafts (CTG)

Locations

Country	Name	City	State
India	SVS Institute of Dental Sciences	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	BL Gain	The displacement from the baseline to 6-months in BL dimensions was calculated and was described as BL gain.	Baseline to 6 months
Primary	Total displacement (TD)	The total displacement (TD) from the baseline to 6-months in MD dimensions was calculated and was described as TD gain.	Baseline to 6 months
Primary	Angle of Displacement (AOD)	The Angle of Displacement (AOD)) from the baseline to 6-months in MD dimensions was calculated and was described as AOD Change.	Baseline to 6 months