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Comparative analysis of clinical outcomes using three different absorbable sutures in impacted third molar surgeries - Randomised control study

Comparative analysis of clinical outcomes using polydioxanone, polyglecaprone 25 AND polyglactin 910 sutures in impacted third molar surgeries - Randomised control study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084923
Enrollment
45
Registered
2025-04-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: Z768- Persons encountering health services in other specified circumstances

Interventions

Intervention1: SUTURE MATERIALS: KNOTLESS BARBED SUTURE MONOFILAMENT ABSORBABLE SUTURE MULTIFILAMENT ABSORBABLE SUTURE Intervention2: Absorbable Knotless Barbed Suture: Its a surgical suture that is

Sponsors

ITS Dental College Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Individuals with at least one impacted mandibular third molar requiring surgical removal. ASA Grade I and II Willingness to abide and comply with the protocol requirement and visits for follow-up

Exclusion criteria

Exclusion criteria: Medically compromised patients Active pus discharge, infection at the operative site Tobacco users Pregnant women

Design outcomes

Primary

MeasureTime frame
The primary outcomes of the study will be: Healing Time Evaluating how quickly the surgical site heals with each suture type. Infection Rates Assessing the incidence of post-operative infections in each group. Post-Operative Pain Measuring pain levels using a standardized pain scale over a set period. Swelling Comparing post-operative edema across the three suture groups. Patient Comfort Assessing factors like irritation, tightness, or discomfort related to the suture material.Timepoint: at 3 days , one week , 10 days and 15 days

Secondary

MeasureTime frame
Patient Comfort Assessing factors like irritation, tightness, or discomfort related to the suture material.Timepoint: at one week , & fifteen days

Countries

India

Contacts

Public ContactDEVYANI SHARMA

ITS DENTAL COLLEGE , HOSPITAL AND RESEARCH CENTRE GREATER NOIDA

himanshubhutiani@gmail.com8076039385

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026