An interventional study of Control group : Coe-pak and Study Group: Reso-pac in Keratinized Tissue Deficiency, sponsored by Damascus University. Completed at 1 site in Syria. Open to participants aged 18 Years to 30 Years. Per ClinicalTrials.gov, last updated 2026-10-27.
Sponsored by Damascus University · Not applicable, Interventional, and Treatment
The periodontal dressing was applied to the donor site of the free gingival graft on the palate to protect the site, reduce postoperative pain, and improve soft tissue healing in the palatal area.
Traditional periodontal dressings require mechanical retention within the interdental spaces and lack bioactive agents that promote healing or reduce pain.
In contrast, the adhesive dressing used in the study group adheres to soft tissues and contains bioactive agents that help reduce pain and enhance healing.
Damascus University is the lead sponsor of 212 studies on the registry; 11 are open to participants now.
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Width of attached gingiva less than 2 mm.
Exclusion Criteria:
\- Control group (Coe-Pack): : Coe-Pak periodontal dressing applied to the palatal donor site immediately after free gingival graft harvesting and maintained for one week.
Other: Control group : Coe-pak
\- Study group (Reso-Pac):Reso-Pac resorbable periodontal dressing applied to the palatal donor site immediately after free gingival graft harvesting and maintained for one week.
Other: Study Group: Reso-pac
\- Control group (Coe-Pack): Coe-Pack dressing is applied to the palatal donor site after harvesting the epithelial graft.
\- Study group (Reso-Pac): Reso-Pac dressing is applied to the palatal donor site after harvesting the epithelial graft.
Outcome MeasuresTitle: Pain Index
The Visual Analog Scale (VAS) was used to assess patients' pain and discomfort daily for one week following treatment. The patient was given a sheet containing a pain scale on which to record their pain level daily. This scale was divided into 100-millimeter increments; a score of 0 at the left end of the scale indicated no pain, while a score of 100 at the right end indicated unbearable pain.
Time frame: Time frame :T1: Day 1 post-surgery , T2 : Day 2 Post-surgery , T3: Day 3 post-surgery , T4: Day 4 post-surgery , T5: Day 5 post-surgery , T6: Day 6 post-surgery, Time Final: Day 7 post-surgery..
Plan to share: No
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.
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