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A novel posterior palatal donor site for autogenous bone harvesting: A prospective case series study

A novel posterior palatal donor site for autogenous bone harvesting: A prospective case series study

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250509001
Enrollment
15
Registered
2025-05-09
Start date
2025-05-06
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

The autogenous bone graft will be harvested from a site that is continuous with the recipient area and thus, the need for an extra surgical site would be eliminated. Bone scraper, ridge preservation, autogenous bone, palatal graft

Interventions

Atraumatic tooth extraction, with flapless technique, using periotom elevator and forceps will be tried to preserve the sockets walls. An envelope flap design will be achieved at the palatal side exte
Experimental Procedure/Surgery
Autogenous palatal bone graft

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Any patient needs dental extraction for maxillary first premolar (1P) and second premolar (2P). 2. Medically fit. 3. Age range between 18-60. 4. Non-smoker or light smoker (< 10 cigarette / day).

Exclusion criteria

Exclusion criteria: 1. Patients with uncontrolled systemic disease involving the bone. 2. Long span edentulous ridge. 3. Age below 18 y or over 60. 4. History of cleft palate. 5. Traumatic extraction and/or oro-antral communication at the time of extraction. 6. Heavy smoking. 7. Acute infection. 8. Previous radiation therapy.

Design outcomes

Primary

MeasureTime frame
Amount of harvested ABG Time of surgery Adequate or not,Time of operation Time of surgery Minutes (min),Primary Implant stability 4 months after surgery Osstell,Secondary Implant stability 8 months after surgery Osstell

Secondary

MeasureTime frame
Surgical access and difficulty Time of surgery Surgeon experience,Surgical complications At the time of operation Clinically,Severity of pain First 7 days after surgery Visual analogue scale (VAS),Post-operative morbidities After surgery Clinically

Countries

Iraq

Contacts

Public ContactFiras Jamil

College of Dentistry, University of Baghdad

dr.firasjamil@gmail.com7901892291

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026