Surgical Management of Interdental Papilla Recession With Advanced Platelet Rich Fibrin or Connec… (NCT05031169) | Clinical Trial Compass
UnknownNot Applicable
Surgical Management of Interdental Papilla Recession With Advanced Platelet Rich Fibrin or Connective Tissue Graft
Egypt32 participantsStarted 2020-09-01
Plain-language summary
deficient interdental papillae witt be surgically reconstructed. in one group, connective tissue graft (SCTG) will be used for papillae augmentation, while in the other group, advanced platelet rich fibrin (A-PRF). the height of the papillae will be measured preoperatively as well as post operatively at 3, 6 ,9 and 12 months.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Be healthy adults older than 18 years of age and presenting at least one deficient papilla with papilla presence index 2 or 3
* Have Interproximal CAL ≤ 3 mm
* Have probing depth ≤ 3mm
* Distance between the alveolar bone crest and contact point is less than 7mm.
Exclusion Criteria:
* Smoking.
* Pregnancy and lactation.
* Carious and non-carious cervical lesion in the involved teeth around the papilla.
* Restoration in teeth around the papilla (filling, crown, bridge, facings, clasp of a partial denture).
* Open contacts and non-vital teeth
* Poor oral hygiene with plaque index \> 20 %.
* Tooth mobility
* History of medication in the previous 3 months
* History of periodontal surgery in the site to be treated in the past 12 months
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.