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dimensional change in gingival graft ,scalpel versus graft

Dimensional changes in free gingival grafts: scalpel versus Er:YAG laser--an rct study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170916036203N3
Enrollment
10
Registered
2018-05-04
Start date
2017-09-23
Completion date
Unknown
Last updated
2018-06-18

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

Conditions

Dimensional changes in gingival graft after 6 months. Disorder of gingiva and edentulous alveolar ridge, unspecified

Interventions

Intervention 1: Intervention group: In these patients, the receptor bed of graft is prepared bye Er: cr: YSGG laser ( manufactured by the United States Biolase company with 2 watts, 50Hz, 60% water an

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Age older than 18 years requires increased attached gingiva width in the mandibular premolar area(Keratinized gingiva less than 2mm or attached gingiva less than 1mm) Patients' health in terms of systemic and periodontal conditions (probe depth less than 3 mm or BOP Grade 1 or less) good plaque control (plaque index less than 20%) Ability to adapt the patient to the study-related processes

Exclusion criteria

Exclusion criteria: 1- heavy smoker (those who smokes more than 10 cigarettes a day) Having a systemic problem that has a negative effect on wound healing. And taking medications that interfere with surgical repair pregnant patients Use of antibiotics over the past 6 months

Design outcomes

Primary

MeasureTime frame
Dimensional changes of free gingival grafts in two substrates prepared with Orbium Laser Er: Cr: YSGG and the Scalpel Common Method. Timepoint: 1st, 3rd and 6th months after surgery. Method of measurement: Image J software (mm2).

Secondary

MeasureTime frame
Duration of surgery. Timepoint: Surgical day. Method of measurement: Time in minutes.;Pain. Timepoint: The first 10 days after surgery. Method of measurement: Questionaire (VAS).;Swelling. Timepoint: The first 10 days after surgery. Method of measurement: questionnaire and patient examination.;Hematoma. Timepoint: the first 10 days after surgery. Method of measurement: questionaire.;Colour Match (brightness parameters). Timepoint: 6 month after surgery. Method of measurement: adobe photoshop.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamed Rahimi

Tehran University of Medical Sciences

hamedr2003@yahoo.com+98 21 8821 3507

Outcome results

None listed

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