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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04772508
Other study ID # 13/395
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2020
Est. completion date March 13, 2021

Study information

Verified date March 2021
Source Maharishi Markendeswar University (Deemed to be University)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

45 sites in 15 patients with periodontal pockets ≥ 5mm were selected. These selected sites were divided into 3 groups as Group A, B and C.


Description:

Group A (Control): 15 sites received only SRP, Group B: 15 sites received SRP with subgingival placement of amnion membrane, Group C: 15 sites received SRP with subgingival placement of Amnion membrane hydrated with Taurine.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date March 13, 2021
Est. primary completion date March 13, 2021
Accepts healthy volunteers No
Gender All
Age group 29 Years to 60 Years
Eligibility Inclusion Criteria: •Systemically healthy patients with sites showing probing depth (PD) = 5mm, clinical attachment level (CAL) = 4 mm, and vertical bone loss = 3 mm on intraoral periapical radiographs with no history of periodontal therapy or use of antibiotics in the preceding 6 months Exclusion Criteria: - Any systemic disease that could influence the outcome of periodontal therapy. - Smokers, alcoholics & patients with other adverse habits. - Pregnant or nursing women. - Any known allergy or hypersensitivity to any product used in the study. - Patients on long term systemic therapy (antibiotics, anti-inflammatory and any other).

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Scaling and root planing
15 sites with periodontal pockets = 5mm received only SRP
Biological:
Amnion membrane
15 sites with periodontal pockets = 5mm received SRP along with placement of amnion membrane.
Drug:
Taurine
15 sites with periodontal pockets = 5mm received SRP along with placement of amnion membrane hydrated with taurine.

Locations

Country Name City State
India Department of Periodontology, M.M. College of Dental Sciences and Research. Ambala Haryana

Sponsors (1)

Lead Sponsor Collaborator
Maharishi Markendeswar University (Deemed to be University)

Country where clinical trial is conducted

India, 

References & Publications (2)

Giris M, Depboylu B, Dogru-Abbasoglu S, Erbil Y, Olgaç V, Alis H, Aykaç-Toker G, Uysal M. Effect of taurine on oxidative stress and apoptosis-related protein expression in trinitrobenzene sulphonic acid-induced colitis. Clin Exp Immunol. 2008 Apr;152(1):102-10. doi: 10.1111/j.1365-2249.2008.03599.x. Epub 2008 Jan 28. — View Citation

Gültekin SE, Sengüven B, Sofuoglu A, Taner L, Koch M. Effect of the topical use of the antioxidant taurine on the two basement membrane proteins of regenerating oral gingival epithelium. J Periodontol. 2012 Jan;83(1):127-34. doi: 10.1902/jop.2011.100568. Epub 2011 May 16. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary TNF-a level TNF-a level in Gingival crevicular fluid changes from baseline to 45 days
Primary Probing pocket depth (PPD) Probing pocket depth at selected site changes from baseline to 45 days
Primary Relative attachment level (RAL) Relative attachment level from stent to base of the pocket changes from baseline to 45 days
Secondary Plaque index (PI) Plaque index (PI) - Silness and Loe 1964 site specific changes from baseline to 45 days
Secondary Gingival index (GI) Gingival index (GI) - Loe and Silness 1963 site specific changes from baseline to 45 days
Secondary Bleeding on probing (BOP) Bleeding on probing (BOP): Muhlemann HR & Son 1971 sit specific changes from baseline to 45 days
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