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effect of biologic dressing on the palatal wound healing

Effect of biologic dressing on the wound healing of the palatal donor site in free gingival graft technique

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016021321069N1
Enrollment
12
Registered
2016-06-13
Start date
2016-04-03
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

palatal wound healing following free gingival graft surgeries. Disorder of gingiva and edentulous alveolar ridge, unspecified

Interventions

Intervention 1: In test group after controlling the bleeding with a wet gauze , the biologic dressing is placed on the donor site ad is sutured to the adjacent area. Intervention 2: In control partici
Treatment - Surgery
In control participants: after harvesting the tissue from the palate, gauze is kept in place to stop Bleeding and the wound will be sutured.
In test group after controlling the bleeding with a wet gauze , the biologic dressing is placed on the donor site ad is sutured to the adjacent area

Sponsors

vice chancellor for research, Tehran University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: healthy subject who needs gingival augmentation by free gingival graft technique in any parts of the gingiva will be included. exclusion criteria: patients with non controlled diabetes;patients with immune deficiency diseases or who received immunosuppressive medications; smokers; pregnant and /or lactating women

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of pain after harvesting graft from palatal area. Timepoint: 7,14 and 21 days after surgery. Method of measurement: VAS ( Visual Analogue Scale) 0= no pain, 10= the most sever pain had been experienced.

Secondary

MeasureTime frame
Healing rate of palatal donor area. Timepoint: 7,14 and 21 days after syrgery. Method of measurement: evaluation of photographies by 2 investigators.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsolmaz akbari

periodontics department of dental school, Tehran University of Medical Science

soolmaz.akbari@gmail.com+98 21 8824 9184

Outcome results

None listed

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