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The Effect of Collagen Matrix Graft on Postoperative Palatal Fistula Formation After Cleft Palate Repair

Primary Purpose

Cleft Lip and Cleft Palate, Cleft Lip, Cleft Alveolus and Cleft Palate, Cleft Palate

Status
Recruiting
Phase
Not Applicable
Locations
Nigeria
Study Type
Interventional
Intervention
Two-flap palatoplasty
Sponsored by
Lagos State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cleft Lip and Cleft Palate focused on measuring cleft palate, palatal fistula, collagen graft

Eligibility Criteria

9 Months - 2 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Non-syndromic cleft palate
  • Must be between nine months to two years
  • Must have not previously had cleft palate surgery
  • Must consent to participate in the study

Exclusion Criteria:

  • All blood dyscrasias
  • All connective tissue dysfunctions

Sites / Locations

  • Lagos University Teaching HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Test group

Control group

Arm Description

The intervention will be primary cleft palate repair using resorbable collagen matrix graft as superpositional graft during approximation of the nasal mucosa and muscular layer in cleft palate repair. The collagen graft with be inserted between the nasal mucosa/ muscular layer and the oral mucosa layer during two-flap palatoplasty.

The intervention will be primary cleft palate repair using two-flap palatoplasty technique without collagen graft

Outcomes

Primary Outcome Measures

Number of participants with postoperative palatal fistula
Palatal fistula will be defined as a patency between the oral and nasal cavities developing postoperatively anywhere along the primary or secondary palate
Number of participants with postoperative palatal fistula
Palatal fistula will be defined as a patency between the oral and nasal cavities developing postoperatively anywhere along the primary or secondary palate
Number of participants with postoperative palatal fistula
Palatal fistula will be defined as a patency between the oral and nasal cavities developing postoperatively anywhere along the primary or secondary palate
Number of participants with postoperative palatal fistula
Palatal fistula will be defined as a patency between the oral and nasal cavities developing postoperatively anywhere along the primary or secondary palate

Secondary Outcome Measures

Number of participants with wound dehiscence
Wound dehiscence will be defined as partial or total separation of previously approximated and sutured surgical wound edges with or without palatal fistula formation.
Number of participants with wound dehiscence
Wound dehiscence will be defined as partial or total separation of previously approximated and sutured surgical wound edges with or without palatal fistula formation.
Number of participants with wound dehiscence
Wound dehiscence will be defined as partial or total separation of previously approximated and sutured surgical wound edges with or without palatal fistula formation.
Number of participants with wound dehiscence
Wound dehiscence will be defined as partial or total separation of previously approximated and sutured surgical wound edges with or without palatal fistula formation.
Number of participants with surgical site inflammation
Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site.
Number of participants with surgical site inflammation
Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site.
Number of participants with surgical site inflammation
Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site.
Number of participants with surgical site inflammation
Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site.
Number of participants with surgical site infection
Surgical site infection will be defined as tenderness and purulent discharge and/or foul smelling odor from surgical site
Number of participants with surgical site infection
Surgical site infection will be defined as tenderness and purulent discharge and/or foul smelling odor from surgical site
Number of participants with surgical site infection
Surgical site infection will be defined as tenderness and purulent discharge and/or foul smelling odor from surgical site
Number of participants with surgical site infection
Surgical site infection will be defined as tenderness and purulent discharge and/or foul smelling odor from surgical site
Surgeon satisfaction
Surgeon satisfaction will assess surgeons' opinion on surgery time (normal/ extended), difficulty of procedure (not difficult/ increased difficulty) and inadvertent tearing of the nasal mucosa (absent/ present).
Psychology of parents towards surgical treatment
Psychology of parents towards surgical treatment will assess parents' psychology towards the aesthetic outcome of the cleft palate repair, its effect on their wards feeding and speech ability postoperatively
Psychology of parents towards surgical treatment
Psychology of parents towards surgical treatment will assess parents' psychology towards the aesthetic outcome of the cleft palate repair, its effect on their wards feeding and speech ability postoperatively
Psychology of parents towards surgical treatment
Psychology of parents towards surgical treatment will assess parents' psychology towards the aesthetic outcome of the cleft palate repair, its effect on their wards feeding and speech ability postoperatively
Psychology of parents towards surgical treatment
Psychology of parents towards surgical treatment will assess parents' psychology towards the aesthetic outcome of the cleft palate repair, its effect on their wards feeding and speech ability postoperatively

Full Information

First Posted
July 2, 2022
Last Updated
October 2, 2023
Sponsor
Lagos State University
Collaborators
University of Lagos, Nigeria
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1. Study Identification

Unique Protocol Identification Number
NCT05454670
Brief Title
The Effect of Collagen Matrix Graft on Postoperative Palatal Fistula Formation After Cleft Palate Repair
Official Title
The Effect of Collagen Matrix Graft on Postoperative Palatal Fistula Formation After Cleft Palate Repair: A Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 10, 2022 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
May 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lagos State University
Collaborators
University of Lagos, Nigeria

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Palatal fistulas are a major burden to surgeons and patients in the management of cleft palate. Their high rate of occurrence and recurrence makes them particularly challenging even to the highly skilled surgeon. Prevention of postoperative palatal fistula is therefore of paramount importance. Closure of the nasal mucosa under tension has been proposed as a major cause of palatal fistula formation. However, depending on the presentation of the cleft palate, it may be impossible to achieve surgical closure with minimal tension. Till date, there is no universally acceptable method of preventing palatal fistula formation following cleft palate repair. And although the use of pre-surgical appliances such as Latham appliance and the use of local and distant tissues to achieve two layer closure have been proposed, the use of a superpositional collagen graft may also be used to achieve closure of the nasal mucosa with minimal or no tension during cleft palate repair. Collagen grafts have the added advantage of being more patient friendly compared to the Latham appliance which requires an initial surgery for appliance insertion before surgical cleft palate repair. They are also less technique sensitive compared to the use of local and distant tissues. The investigators therefore aim to provide high level scientific evidence of the effectiveness of collagen graft in the prevention of postoperative palatal fistula.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cleft Lip and Cleft Palate, Cleft Lip, Cleft Alveolus and Cleft Palate, Cleft Palate
Keywords
cleft palate, palatal fistula, collagen graft

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study will be a parallel randomized controlled study involving two groups of participants. The test group will include participants with who will undergo cleft palate repair with collagen graft used as superpositional graft between the nasal mucosa/muscle layer and the oral mucosa layer when two-flap palatoplasty is performed while the control group will include participants who undergo two-flap palatoplasty without the use of collagen graft
Masking
ParticipantOutcomes Assessor
Masking Description
This study will be a double-blind randomized controlled study. After random allocation, the participants (parents/ patients) will be unaware of the study group they belong to. Also, the surgeon assessing postoperative outcomes will not perform the surgery and will be unaware of the study group of the participant being examined. Since the collagen graft will be placed between the nasal/ muscular layers and the oral layer, it is expected that after apposition of the oral layer, no collagen matrix will be visible intraorally to reveal the study group of participants.
Allocation
Randomized
Enrollment
46 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Test group
Arm Type
Experimental
Arm Description
The intervention will be primary cleft palate repair using resorbable collagen matrix graft as superpositional graft during approximation of the nasal mucosa and muscular layer in cleft palate repair. The collagen graft with be inserted between the nasal mucosa/ muscular layer and the oral mucosa layer during two-flap palatoplasty.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
The intervention will be primary cleft palate repair using two-flap palatoplasty technique without collagen graft
Intervention Type
Procedure
Intervention Name(s)
Two-flap palatoplasty
Intervention Description
Two-flap palatoplasty used to correct cleft palate defect. The cleft palate is closed by separation of the nasal and the oral mucosa layers. Then approximation of the nasal mucosa layer, muscle layer is secured in the posterior palate and then the oral mucosa layer is secured
Primary Outcome Measure Information:
Title
Number of participants with postoperative palatal fistula
Description
Palatal fistula will be defined as a patency between the oral and nasal cavities developing postoperatively anywhere along the primary or secondary palate
Time Frame
24 hours post operatively
Title
Number of participants with postoperative palatal fistula
Description
Palatal fistula will be defined as a patency between the oral and nasal cavities developing postoperatively anywhere along the primary or secondary palate
Time Frame
Seven days post operatively
Title
Number of participants with postoperative palatal fistula
Description
Palatal fistula will be defined as a patency between the oral and nasal cavities developing postoperatively anywhere along the primary or secondary palate
Time Frame
Two weeks post operatively
Title
Number of participants with postoperative palatal fistula
Description
Palatal fistula will be defined as a patency between the oral and nasal cavities developing postoperatively anywhere along the primary or secondary palate
Time Frame
One month post operatively
Secondary Outcome Measure Information:
Title
Number of participants with wound dehiscence
Description
Wound dehiscence will be defined as partial or total separation of previously approximated and sutured surgical wound edges with or without palatal fistula formation.
Time Frame
24 hours post operatively
Title
Number of participants with wound dehiscence
Description
Wound dehiscence will be defined as partial or total separation of previously approximated and sutured surgical wound edges with or without palatal fistula formation.
Time Frame
Seven days post operatively
Title
Number of participants with wound dehiscence
Description
Wound dehiscence will be defined as partial or total separation of previously approximated and sutured surgical wound edges with or without palatal fistula formation.
Time Frame
Two weeks post operatively
Title
Number of participants with wound dehiscence
Description
Wound dehiscence will be defined as partial or total separation of previously approximated and sutured surgical wound edges with or without palatal fistula formation.
Time Frame
One month post operatively
Title
Number of participants with surgical site inflammation
Description
Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site.
Time Frame
24 hours post operatively
Title
Number of participants with surgical site inflammation
Description
Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site.
Time Frame
Seven days post operatively
Title
Number of participants with surgical site inflammation
Description
Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site.
Time Frame
Two weeks post operatively
Title
Number of participants with surgical site inflammation
Description
Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site.
Time Frame
One month post operatively
Title
Number of participants with surgical site infection
Description
Surgical site infection will be defined as tenderness and purulent discharge and/or foul smelling odor from surgical site
Time Frame
24 hours post operatively
Title
Number of participants with surgical site infection
Description
Surgical site infection will be defined as tenderness and purulent discharge and/or foul smelling odor from surgical site
Time Frame
Seven days post operatively
Title
Number of participants with surgical site infection
Description
Surgical site infection will be defined as tenderness and purulent discharge and/or foul smelling odor from surgical site
Time Frame
Two weeks post operatively
Title
Number of participants with surgical site infection
Description
Surgical site infection will be defined as tenderness and purulent discharge and/or foul smelling odor from surgical site
Time Frame
One month post operatively
Title
Surgeon satisfaction
Description
Surgeon satisfaction will assess surgeons' opinion on surgery time (normal/ extended), difficulty of procedure (not difficult/ increased difficulty) and inadvertent tearing of the nasal mucosa (absent/ present).
Time Frame
within the first 24 hours post operatively
Title
Psychology of parents towards surgical treatment
Description
Psychology of parents towards surgical treatment will assess parents' psychology towards the aesthetic outcome of the cleft palate repair, its effect on their wards feeding and speech ability postoperatively
Time Frame
24 hours post operatively
Title
Psychology of parents towards surgical treatment
Description
Psychology of parents towards surgical treatment will assess parents' psychology towards the aesthetic outcome of the cleft palate repair, its effect on their wards feeding and speech ability postoperatively
Time Frame
Seven days post operatively
Title
Psychology of parents towards surgical treatment
Description
Psychology of parents towards surgical treatment will assess parents' psychology towards the aesthetic outcome of the cleft palate repair, its effect on their wards feeding and speech ability postoperatively
Time Frame
Two weeks post operatively
Title
Psychology of parents towards surgical treatment
Description
Psychology of parents towards surgical treatment will assess parents' psychology towards the aesthetic outcome of the cleft palate repair, its effect on their wards feeding and speech ability postoperatively
Time Frame
One month post operatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
9 Months
Maximum Age & Unit of Time
2 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Non-syndromic cleft palate Must be between nine months to two years Must have not previously had cleft palate surgery Must consent to participate in the study Exclusion Criteria: All blood dyscrasias All connective tissue dysfunctions
Facility Information:
Facility Name
Lagos University Teaching Hospital
City
Lagos
ZIP/Postal Code
12003
Country
Nigeria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wasiu L Adeyemo, PhD
Phone
8023115885
Ext
234
Email
lanreadeyemo@yahoo.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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The Effect of Collagen Matrix Graft on Postoperative Palatal Fistula Formation After Cleft Palate Repair

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