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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03180658
Other study ID # 81600868
Secondary ID
Status Recruiting
Phase N/A
First received May 29, 2017
Last updated June 7, 2017
Start date May 1, 2017
Est. completion date July 1, 2020

Study information

Verified date June 2017
Source Peking University
Contact qiao jing, doctor
Phone 86-13241892143
Email donaldshushu@aliyun.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objective: To compare the effect of guided tissue regeneration (GTR) + concentrated growth factors (CGF) + bone graft and CGF + bone graft in the treat of II° furcations of human mandibular molars. Methods: At least thirty II°furcation involvements in mandibular molars will be included and randomly divided into two groups. The experimental group will accept GTR + CGF + bone graft therapy, and the control group will accept CGF + bone graft therapy. The clinical examination and cone beam computed tomography (CBCT) will be performed at baseline and 1 year post-surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date July 1, 2020
Est. primary completion date May 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- IIĀ° furcation involvements in mandibular molars

- after periodontal therapy.

Exclusion Criteria:

- not healthy

Study Design


Intervention

Procedure:
GTR + CGF + bone graft
Guided tissue regeneration (GTR) combined with CGF and bone graft to treat mandibular furcation involvements
CGF + bone graft
CGF combined with bone graft to treat mandibular furcation involvements

Locations

Country Name City State
China Peking university School and Hospital of Stomatology Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Jing Qiao

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary clinical measurement Probing depth 1 year
Primary clinical parameter clinical attachment loss 1 year
Secondary radiographic parameter cone beam computerized tomographic scanning 1 year
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