Comparison of two methods of graft in patients who are candidate for gingival grafts

Comparison of increasing the width and thickness of keratinized gingiva in two methods of connective tissue graft and graft by composition of collagen and rich plasma in patients who are candidate for gingival grafts

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201202018723N1

Enrollment

Registered

2012-04-22

Start date

2012-02-20

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

Inadequate width and thickness of keratinized gingiva. Gingival recession

Interventions

Intervention 1: intervention group: surgery of graft of stypro plus platelet rich plasma plus platelet rich fibrin. Intervention 2: control group: surgery of gingival graft (connective tissue graft).

Treatment - Other

intervention group: surgery of graft of stypro plus platelet rich plasma plus platelet rich fibrin

control group: surgery of gingival graft (connective tissue graft)

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: inclusion criteria:patients with inadequate width(2 mm or less) and thickness(1 mm or less) of keratinized gingiva bilaterally at buccal in one root teeth;without muscle attachment; with 5 to 7 mm depth of the vestible; adjacent teeth have enough width and thickness of keratinized gingiva. exclusion criteria:pregnancy;clotting disorders;diabete;cardiovascular problems;hypertension;radiotherapy;cancer;other systemic disorders

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Width of keratinized gingiva. Timepoint: 1,2 and 3 months after intervention. Method of measurement: rolling and logul solution.;Thickness of keratinized gingiva. Timepoint: 1,2 and 3 months after intervention. Method of measurement: with endodontic files.	—

Secondary

Measure	Time frame
Pain. Timepoint: everyday until one week after surgery. Method of measurement: with VAS.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSamira Esmailzadeh

Fars University of Medical Sciences

esmaeilzad@sums.ac.irsamira.esmailzadeh@yahoo.com+98 936 888 5061

Outcome results

None listed

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