To evaluate the efficacy of low level laser therapy in coronally advanced flap with collagen membrane in the treatment of gingival recession.

Phase 2

Recruiting

• Conditions: Localised periodontitis.Millers class I or Class II gingival recession

• Registration Number: CTRI/2020/01/022708
• Lead Sponsor: DrMaydina Achom

Brief Summary

comparative evaluationof the efficacy of coronally advanced flap using collagen membrane with or without low level laser therapy in the treatment of millers class I or II gingival recession. Standardised clinical parameters measured are gingival index, plaque index, width of keratinized gingiva, gingival recession height, pocket probing depth,relative clinical attachment level, wound healing and degree of pain level.

Detailed Description

Not available

Study Timeline

• Study Start: 2020-01-13
• Last Update Posted: 2020-01-13

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Systemically healthy subjects.
• Subjects with age between 18-55 years old.
• Patients having isolated Miller’s class I or class II Gingival recession with adequate width of attached Gingival.
• Subjects who were willing to comply with all the study related procedure and willing to sign the informed consent form.

Exclusion Criteria

• Medically compromised Patients.
• Patients with any history of allergy to the material used in this study.
• Patients who are on antibiotics or antimicrobial therapy, immunosuppressant drug for the last 3 months.
• Patients on any drug therapy which is known to influence the periodontium.
• Patients who have undergone any type of periodontal surgical procedure 6 months prior to the initial examination.
• Patients who are active tobacco users.
• Patient showing pulpal exposures, non-vital tooth or active caries or restoration on root surface of tooth to be treated.
• Pregnant and lactating females.
• Supra-erupted tooth; High frenal attachment.
• Subject unable to provide informed consent.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Gingival index, Plaque index, Pocket Probing depth,Gingival recession height, Width of keratinised gingiva,Relative clinical attachment level,Wound healing and Pain score	baseline, 1 month and 3 months

Secondary Outcome Measures

Name	Time	Method
Gingival index, Plaque index, Pocket Probing depth.	baseline, 1 month and 3 months

Trial Locations

Locations (1)

ITS center for dental science and research; 🇮🇳 Ghaziabad, UTTAR PRADESH, India

ITS center for dental science and research

🇮🇳Ghaziabad, UTTAR PRADESH, India

DrMaydina Achom

Principal investigator

7005611421

maydinaachom@gmail.com