Double Closure of Nasal Layer in Alveolar Cleft Grafting

Sponsor
Tanta University (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05988086
Collaborator
(none)
24
1
2
10.2
2.4

Study Details

Study Description

Brief Summary

The aim of this prospective study is to evaluate both clinically and radiologically the efficacy of using autologous platelets rich fibrin versus collagen membrane for nasal layer closure in secondary alveolar cleft repair.

Condition or Disease Intervention/Treatment Phase
  • Procedure: platelet rich fibrin
  • Procedure: collagen membrane
N/A

Detailed Description

Patients and methods: Twenty-four patients with alveolar clefts will be included in this study. The patients will be evaluated with age ranging between (7 - 12) years. The patients will be received, clinically and radiologically examined, and managed at the Oral and Maxillofacial surgery Department, Faculty of Dentistry, Tanta University.

The selected children should possess the following criteria: Their permanent canines either not or partially erupted, has no systemic disorder which can affect the grafting outcome and healing process such as juvenile diabetes mellitus, kidney, liver, or blood diseases and has no associated craniofacial syndromes. The patients will be classified into two groups according to incorporation of autologous platelet rich fibrin or collagen membrane for nasal layer closure with the grafting material, as follow: Group 1: This will include 12 children in whom nasal layer of alveolar cleft will be repaired using autologous platelet rich fibrin with autogenous chin bone. Group 2: This will include 12 children in whom nasal layer of alveolar cleft will be repaired using collagen membrane with autogenous chin bone.

Preoperative evaluation of alveolar cleft site:

all patients will be examined clinically and radiologically. Clinical examination: This will consider the stability of maxillary segments, presence of old scar, asymmetry of the alar base, presence of oronasal fistula, and the presence of erupting teeth in the cleft.

Radiological examination: Panoramic radiographs will be done for each patient and examined as regard: the morphology of the cleft area, the size of the cleft side, the presence or absence of permanent lateral incisor and canine, the development of root length, and stage of eruption of permanent canine and lateral incisor. In addition, Axial computed tomography (CT) scans will be done for each patient to assess and measure local bone mineral density of grafted alveolar bone cleft.

Postoperative evaluation of the grafted site:

The grafted site will be evaluated clinically for healing condition at the follow up periods (1st week, then 1st , 3rd ,6th ,and 9th month postoperatively) ; regarding the presence of inflammation or infection , the soft tissue scar overlying the bone graft , tenderness of bone graft site , recurrence of oronasal fistula , alveolar ridge contour in cleft region and eruption of cleft related teeth . Radiological evaluation will be done for each patient using Axial computed tomography (CT) scans at the follow up period (3rd and 9th month postoperatively) to assess and measure local bone mineral density.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
24 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Evaluation of Using Platelet Rich Fibrin Versus Collagen Membrane for Enhancing Healing of Secondary Grafted Alveolar Cleft
Actual Study Start Date :
Oct 10, 2022
Actual Primary Completion Date :
Mar 10, 2023
Anticipated Study Completion Date :
Aug 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Group 1: platelet rich fibrin

Group 1: This will include 12 children in whom nasal layer of alveolar cleft will be repaired using autologous platelet rich fibrin with autogenous chin bone.

Procedure: platelet rich fibrin
12 children in whom nasal layer of alveolar cleft will be repaired using autologous platelet rich fibrin with autogenous chin bone.

Active Comparator: Group 2:collagen membrane

Group 2: This will include 12 children in whom nasal layer of alveolar cleft will be repaired using collagen membrane with autogenous chin bone.

Procedure: collagen membrane
12 children in whom nasal layer of alveolar cleft will be repaired using collagen membrane with autogenous chin bone.

Outcome Measures

Primary Outcome Measures

  1. visual analogue scale [1 month]

    0 representing no pain and 10 representing the highest level of pain

  2. inflammation score scale [1 month]

    0 no inflammation, 1-3 mild inflammation,4-7 moderate inflammation,8-10 severe inflammation

  3. density of bone [1 month]

    density of bone to measure (D1,D2,D3,D4) Frome 150HU to 1250HU

Secondary Outcome Measures

  1. bone mineral density. [9 months]

    density of bone to measure (D1,D2,D3,D4) Frome 150HU to 1250HU

Eligibility Criteria

Criteria

Ages Eligible for Study:
7 Years to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. patients with unilateral alveolar cleft

  2. the patient's permenant canines either not or partially erupted

  3. medically free patients

Exclusion Criteria:
  1. patients with bilateral alveolar cleft

  2. medically compromised patients

  3. Any associated craniofacial syndromes.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Egypt Tanta Egypt 3111

Sponsors and Collaborators

  • Tanta University

Investigators

  • Principal Investigator: Marwa T Ibrahim, lecturer, Tanta University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Marwa Taha Ibrahim, lecturer, Tanta University
ClinicalTrials.gov Identifier:
NCT05988086
Other Study ID Numbers:
  • R-OS-9-22-1
First Posted:
Aug 14, 2023
Last Update Posted:
Aug 14, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Marwa Taha Ibrahim, lecturer, Tanta University

Study Results

No Results Posted as of Aug 14, 2023