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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05454670
Other study ID # ADM/DST/HREC/VOL.XVII/763
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 10, 2022
Est. completion date May 2024

Study information

Verified date October 2023
Source Lagos State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 46
Est. completion date May 2024
Est. primary completion date March 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 9 Months to 2 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Two-flap palatoplasty
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

Locations

Country Name City State
Nigeria Lagos University Teaching Hospital Lagos

Sponsors (2)

Lead Sponsor Collaborator
Lagos State University University of Lagos, Nigeria

Country where clinical trial is conducted

Nigeria, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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 24 hours post operatively
Primary 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 Seven days post operatively
Primary 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 Two weeks post operatively
Primary 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 One month post operatively
Secondary 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. 24 hours post operatively
Secondary 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. Seven days post operatively
Secondary 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. Two weeks post operatively
Secondary 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. One month post operatively
Secondary Number of participants with surgical site inflammation Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site. 24 hours post operatively
Secondary Number of participants with surgical site inflammation Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site. Seven days post operatively
Secondary Number of participants with surgical site inflammation Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site. Two weeks post operatively
Secondary Number of participants with surgical site inflammation Surgical site inflammation will be defined as tenderness, redness, swelling and/or differential warmth from surgical site. One month post operatively
Secondary 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 24 hours post operatively
Secondary 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 Seven days post operatively
Secondary 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 Two weeks post operatively
Secondary 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 One month post operatively
Secondary 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). within the first 24 hours post operatively
Secondary 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 24 hours post operatively
Secondary 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 Seven days post operatively
Secondary 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 Two weeks post operatively
Secondary 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 One month post operatively
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