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Official title Factors Influencing Postoperative Pain After Gingival Graft Harvesting
ClinicalTrials.gov ID: NCT07377370
What this study is testing
- What it's testing
- This prospective cohort study aims to evaluate patient-related, psychological, and clinical factors influencing postoperative pain following gingival graft harvesting from the palate. Consecutive adult patients requiring mucogingival surgery for root coverage or soft tissue augmentation around teeth or dental implants will be recruited at the Clínica Universitària d'Odontologia of Universitat Internacional de Catalunya (Barcelona, Spain).
- This is a blinded study.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older. Healthy volunteers may be eligible.
You may be able to join if
- Patients requiring mucogingival surgery for gingival augmentation or root coverage purposes
- Systemically healthy individuals aged 18 years or older
- Healthy periodontal status according to the AAP/EFP definition
- Full-mouth plaque score (FMPS) and full-mouth bleeding score (FMBS) ≤ 20%
You likely can't join if
- Pregnancy or lactation
- Self-reported smoking ≥10 cigarettes/day
- Presence of metabolic or systemic diseases that negatively affect soft tissue healing
- Use of medications that may interfere with wound healing
- Chronic pain disorders (e.g., fibromyalgia)
- Psychiatric diagnoses
See the full eligibility criteria
- Patients requiring mucogingival surgery for gingival augmentation or root coverage purposes
- Systemically healthy individuals aged 18 years or older
- Healthy periodontal status according to the AAP/EFP definition
- Full-mouth plaque score (FMPS) and full-mouth bleeding score (FMBS) ≤ 20%
- Pregnancy or lactation
- Self-reported smoking ≥10 cigarettes/day
- Presence of metabolic or systemic diseases that negatively affect soft tissue healing
- Use of medications that may interfere with wound healing
- Chronic pain disorders (e.g., fibromyalgia)
- Psychiatric diagnoses
- Regular use of analgesics, antidepressants, anxiolytics, or opioids
- Allergy to the study medication (Ibuprofen)
- History of grafting within the past 6 months
- Ongoing orthodontic therapy
The study team makes the final eligibility decision.
Where it's taking place
- Barcelona, Sant Cugat Del Valles, Spain
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Barcelona, Sant Cugat Del Valles, Spain. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.