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Surgical covering of the exposed tooth root using dehydrated amniotic membrane in the lower front teeth

Evaluation Of Dehydrated Amniotic Membrane (Amnioguard®) On Root Coverage Of Lower Anteriors- A Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/08/009354
Enrollment
10
Registered
2017-08-11
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

Health Condition 1: null- Gingival Recession

Interventions

Intervention1: Dehydrated Amniotic Membrane Amnio guard: Biocover Laborateries Karnal Control Intervention1: nil: nil

Sponsors

JSS Dental College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients who had signed an informed consent. 2. Patients who were systemically healthy patients, both males and females in the age range of 18-50 years. 3. Patients with recession in the mandibular anterior region with Millerâ??s class I or II gingival recessions. 4. Patients with recession depth of >=3mm but less than 5mm. 5. Patients with well aligned teeth. 6. Patients who were able to and willing to follow study procedures and instructions. 7. Patients who were compliant and maintained good plaque control.

Exclusion criteria

Exclusion criteria: 1. Patients who did not provide consent for the study. 2. Patients who had gingival recession (class III and IV) with interdental bone loss. 3. Thin gingival biotype ( 4. Teeth with restored cervical abrasions. 5. Pregnant/lactating women. 6. Patients who were known smokers or who were using smokeless tobacco. 7. Patients who had root caries. 8. Patients with any immunologic disease and who are currently receiving or have received within two months prior to study entry, systemic corticosteroids, immunosuppressive agents, radiation therapy, and/or chemotherapy which would compromise wound healing and preclude periodontal surgery.

Design outcomes

Primary

MeasureTime frame
To evaluate the regenerative potential of dehydrated amniotic membrane using the following clinical parameters: Percentage of root coverage Gain in width of keratinized gingiva Improvement in clinical attachment level Timepoint: At 1 week ,3months and 6 months—

Secondary

MeasureTime frame
2. To assess esthetic outcome following the use of dehydrated amniotic membrane.Timepoint: 6 months—

Countries

India

Contacts

Public ContactDedeepya Gudivada

jss dental college and hospital

sheelagujjari@gmail.com9986176328

Outcome results

None listed

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