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Evaluation of two techniques of free gingival graft and palatal pedicle graft in soft tissue around the implant.

Comparison of Free Gingival Graft and Palatal Pedicle Graft Technique in peri-implant soft tissue phenotype modification in patients with implants in upper jaw

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221226056930N1
Enrollment
34
Registered
2023-03-18
Start date
2023-02-20
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Comparison of free gingival graft and palatal pedicle graft.

Interventions

Intervention 1: Intervention group: Palatal pedicle graft. Intervention 2: Control group: Free gingival graft.

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1patinets age over 18 years old. 2.Healthy in systemic and periodontal condition. 3.patients with stable implants 4. patients with adequate thickness of palate for graft harvesting. 5.patients with keratinized tissue width deficiency.

Exclusion criteria

Exclusion criteria: patients with history of radiotherapy or periodontitis.2. pregnant women or patients with a history more than 10-cigarrete smoking per day.3.patients who are undertreatment of drugs affecting periodontal tissue and wound healing.4.patients with a history of soft tissue grafting in site of surgery

Design outcomes

Primary

MeasureTime frame
Keratinized tissue width. Timepoint: Before intervention, 1month, 3month. Method of measurement: University of North California-15 probe.

Secondary

MeasureTime frame
Soft tissue surface shrinkage around implant. Timepoint: Before intervention, 1month after intervention, 3months after intervention. Method of measurement: Image j software.;Vestibular depth changes. Timepoint: Before intervention, 1month after intervention, 3months after intervention. Method of measurement: University of North California-15 probe.;Numeric analogue scale. Timepoint: Before intervention,1month after intervention, 3months after intervention. Method of measurement: Likert scale.;Amount of the analgesic pill used. Timepoint: Before intervention,1month after intervention, 3months after intervention. Method of measurement: Note in the postoperative form provided to the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Khoshkhou Titkanlou

Tehran University of Medical Sciences

burntgeneration74@gmail.com+98 915 219 8011

Outcome results

None listed

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