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Applicability of Fibrin Glue in closure of nasal mucosa in bone grafting of alveolar clefts

Applicability of Fibrin Glue in closure of nasal mucosa in bone grafting of alveolar clefts

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201103055972N1
Enrollment
15
Registered
2011-06-30
Start date
2011-04-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Alveolar cleft. Cleft hard palate, Unspecified cleft palate with bilateral cleft lip, Unspecified cleft palate with unilateral cleft lip

Interventions

Intervention 1: Intervention group: standard surgical treatment with an exception of closure of the nasal mucosa with fibrin glue instead of standard suturing technique. Intervention 2: Control group:
Treatment - Surgery
Treatment - Drugs
Intervention group: standard surgical treatment with an exception of closure of the nasal mucosa with fibrin glue instead of standard suturing technique
Control group: standard surgical treatment including the closure of the nasal mucosa with sutures

Sponsors

Isfahan University of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
9 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: age of 9 years old and more, no systemic disease, no previous surgical treatment of the same problem, unilateral alveolar cleft, complete mental health Exclusion criteria: less than 9 years old, any previous bone grafting in the cleft area, any systemic disease, bilateral alveolar cleft, any mental or cognitive disease

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Incidence of post operative infection. Timepoint: during the 3-months healing time period. Method of measurement: clinical observation.;Incidence of postoperative wound dehicence. Timepoint: during the 3-months period of healing phase. Method of measurement: clinical observation.

Primary

MeasureTime frame
Bone healing in graft area. Timepoint: 1 and 3 months after operation. Method of measurement: radiographic and clinical examination.;Duration of the procedure. Timepoint: At the end of the surgery. Method of measurement: timer ( minute).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBijan Movahedian Attar

Isfahan University of Medical Sciences

b_movahedian@dnt.mui.ac.ir+98 31 1792 2854

Outcome results

None listed

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