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

Comparative evaluation of the efficacy of coronally advanced flap using collagen membrane with or without low level laser therapy in the treatment of Millers class I and class II gingival recession treatment-A Clinical Study.

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/01/022708

Enrollment

Registered

2020-01-13

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

None listed

Interventions

Intervention1: coronally advanced flap with collagen membrane and Low level laser therapy: coronally advanced flap with collagen membrane and low level laser therapy in the treatment of miller class I

Eligibility

Inclusion criteria

Inclusion criteria: 1. Systemically healthy subjects. 2. Subjects with age between 18-55 years old. 3. Patients having isolated Millerâ??s class I or class II Gingival recession with adequate width of attached Gingival. 4. Subjects who were willing to comply with all the study related procedure and willing to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Medically compromised Patients. 2. Patients with any history of allergy to the material used in this study. 3. Patients who are on antibiotics or antimicrobial therapy, immunosuppressant drug for the last 3 months. 4. Patients on any drug therapy which is known to influence the periodontium. 5. Patients who have undergone any type of periodontal surgical procedure 6 months prior to the initial examination. 6. Patients who are active tobacco users. 7. Patient showing pulpal exposures, non-vital tooth or active caries or restoration on root surface of tooth to be treated. 8. Pregnant and lactating females. 9. Supra-erupted tooth; High frenal attachment. 10. Subject unable to provide informed consent.

Design outcomes

Primary

Measure	Time frame
Gingival index, Plaque index, Pocket Probing depth,Gingival recession height, Width of keratinised gingiva,Relative clinical attachment level,Wound healing and Pain scoreTimepoint: baseline, 1 month and 3 months	—

Secondary

Measure	Time frame
Gingival index, Plaque index, Pocket Probing depth.Timepoint: baseline, 1 month and 3 months	—

Countries

India

Contacts

Public ContactDr Maydina Achom

I.T.S CDSR

nikhilsharma@its.edu.in9818077799

Outcome results