Randomized Clinical and Radiographic Study (NCT06609720) | Clinical Trial Compass
CompletedNot Applicable
Randomized Clinical and Radiographic Study
Egypt32 participantsStarted 2021-03-01
Plain-language summary
Randomized clinical and radiographic trial
Who can participate
Age range35 Years – 55 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
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Presence of class II and/or ΙΙΙ furcation defects in mandibular first or second molars according to criteria outlined by Hamp et. al. 1975.
* Horizontal probing depth ≥3 mm using Naber's probe.
* Clinical attachment level ≥3 mm measured from cemento-enamel junction (CEJ) till the deepest probing depth.
* Evidence of radiolucency in the furcation area on panoramic radiograph.
* Patients who will be assigned for groups (I and II) should present with teeth required for extraction due to advanced periodontal bone loss or other indications such as hopeless wisdom teeth or orthodontic indications or unrestorable fractured teeth as a source for autogenous dentin graft (ADG).
Exclusion Criteria:
* Medically compromised patients and systemic conditions precluding periodontal surgery.
* Mandibular first or second molars with root caries or endodontic treatment.
* Smokers, diabetics, pregnant or lactating women.
* History of chemotherapy, radiotherapy in head and/or neck region.
* Bisphosphonate therapy.
What they're measuring
1
Probing pocket depth
Timeframe: Measured at baseline, 6 months and 12 months
2
Clinical attachment level
Timeframe: Measured at baseline, 6 months and 12 months
3
Bleeding on probing
Timeframe: Measured at baseline, 6 months and 12 months