Comparison of several surgical stents for reducing postoperative pain in palatal donor sites for gingival grafting

Comparison of different methods for palatal surgical stent to reduce donor site morbidity in periodontal plastic surgery

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0010730

Enrollment

Registered

2025-07-08

Start date

2023-11-02

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

None listed

Interventions

Medical Device : Those who voluntarily signed the clinical study consent form and met the inclusion criteria were enrolled in this clinical study. The subjects were randomly assigned to the experiment

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) age > 18 years; 2) gingival recession in multiple teeth; 3) loss of keratinized gingiva around the implant site requiring soft tissue grafting; 4) no systemic diseases contraindicating surgical procedures or compromising wound healing; and 5) healthy or stable periodontal condition.

Exclusion criteria

Exclusion criteria: 1) pregnancy, 2) nursing patients, 3) uncontrolled systemic diseases, 4) alcoholism and drug addiction, and 5) untreated periodontal disease.

Design outcomes

Primary

Measure	Time frame
Oral Health Impact Profile-14 (OHIP-14)	—

Secondary

Measure	Time frame
Patient-Reported Outcome Measures (PROMs) using the visual analog scale (VAS)	—

Countries

Korea, Republic of

Contacts

Public ContactDong-Woon Lee

Wonkwang University Dental Hospital

dongden@daum.net+82-63-859-2966

Outcome results