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Sutureless technique in Implant placement

Evaluation and comparison of the efficacy of autologous fibrin glue with 4-0 resorbable mono filament sutures following implant placement-a randomized clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076348
Enrollment
24
Registered
2024-11-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

None listed

Interventions

Intervention1: autologous fibrin glue: 10 ml of patient blood was collected in sterile 0.9% sodium citrate containing vacutainers for autologous fibrin glue preparation and centrifuged at 3000 rpm for

Sponsors

Dr Ankita Priya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with adequate oral hygiene status. 2.No active periodontal disease present. 3.Patients requiring the replacement of one or more non-restorable teeth with sufficient bone volume will be selected for the study. 4.Patients willing to provide informed consent and maintain adequate oral hygiene. 5.Patients with good compliance to attend follow-ups.

Exclusion criteria

Exclusion criteria: 1.Patients with uncontrolled systemic diseases that might preclude the use of dental implants. 2.Patients with autoimmune diseases or psychiatric disorders. 3.Patients undergoing or who have undergone radiation therapy and chemotherapy to the head and neck region within the last 12 months. 4.Patients with poor oral hygiene. 5.Alcoholics, drug abusers, or heavy smokers. 6.Pregnant or lactating women. 7.Insufficient bone volume or damage to the cortical plate after extraction. 8.Patients who are unable to provide informed consent at the time of the procedure.

Design outcomes

Primary

MeasureTime frame
1. Wound Healing Index 2. Histological characteristics of wound Healing 3. Crestal bone levelsTimepoint: Wound healing index- 1,7,30 days histological characteristics of wound healing- 90 days Crestal bone levels- day 0 and 90 days

Secondary

MeasureTime frame
1. wound healing characterstics by punch biopsy 2. crestal bone levelsTimepoint: at baseline and 3 months

Countries

India

Contacts

Public ContactDr Rahul Chopra

I.T.S DENTAL COLLEGE ,GHAZIABAD

vids1981@gmail.com9489038724

Outcome results

None listed

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