Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 9:21 PM
Ignite Modification Date:
2025-12-24 @ 9:21 PM
NCT ID:
NCT02659904
Eligibility Criteria:
Inclusion Criteria:
* All individuals received oral hygiene instructions and full-mouth scaling was performed. -They were instructed to perform a non-traumatic brushing technique (Roll) using an ultra-soft toothbrush
* Individuals were re-evaluated at 8 weeks after initial therapy, and only full mounth plaque score and full mounth bleeding score \<15% were enrolled to the surgical procedure
* mucogingival defects which for soft tissue graft application were indicated
* For Less than 2 mm group, between 2.5 and 3.4 mm palatal thickness at each measurement points before graft harvesting
* For 2 mm or more group, between 3.5 and 4.4 mm palatal thickness at each measurement points before graft harvesting.
Exclusion Criteria:
* periapical or palatal pathologies,
* absence teeth from canine to first molar,
* excessive forces including mechanical forces from orthodontics and occlusion,
* systemic diseases that would contraindicate for periodontal surgery or interfere with tissue healing, chronic high-dose steroid therapy, radiation or immunosuppressive therapy, pregnancy, lactation, smoking, or allergy or sensitivity to any drug
* Study participants had no history of drug therapy known to interfere with healing and to cause gingival enlargement
* Individuals who had complication such as bleeding, necrosis and delay healing during or after surgery were excluded from the study.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT02659904
Study Brief:
Protocol Section:
NCT02659904