Evaluating bentonite clay gel for bone regeneration in dental defects

Assessing the Clinical Efficacy of Bentonite Clay Gel on Bone Regeneration in the Treatment of Intra-bony Defects: A Clinico-radiograph Study

Not applicable Interventional SVS Institute of Dental Sciences · NCT06439264

This study is testing if a new bentonite clay gel mixed with a bone-building material can help people heal better after dental surgery for bone defects compared to just using the bone-building material alone.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment24 (estimated)
Ages18 Years and up
SexAll
SponsorSVS Institute of Dental Sciences Academic / other
Drugs / interventionschemotherapy
Locations1 site (Mahbūbnagar, Telangana)
Trial IDNCT06439264 on ClinicalTrials.gov

What this trial studies

This study aims to assess the effectiveness of bentonite clay gel combined with hydroxyapatite in promoting bone regeneration in patients with intra-bony defects. Participants will undergo flap surgery, where the test group will receive the bentonite gel with hydroxyapatite, while the control group will receive only hydroxyapatite. The study will compare the clinical and radiographic outcomes between the two groups to determine the efficacy of the bentonite gel treatment.

Who should consider this trial

Good fit: Ideal candidates are systemically healthy adults over 18 years with specific types of intra-bony defects and probing pocket depths of 5mm or more.

Not a fit: Patients who are medically compromised, under 18 years old, pregnant, heavy smokers, or have undergone radiotherapy or chemotherapy may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could enhance bone regeneration in dental procedures, leading to improved patient outcomes.

How similar studies have performed: While the use of hydroxyapatite is established, the specific combination with bentonite clay gel is novel and has not been extensively tested in similar studies.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Systemically healthy male and female patients of age \>18 years
2. two-walled or three-walled intrabony defects and
3. probing pocket depths (PPD) of ≥ 5mm.

Exclusion Criteria:

1. Medically compromised patients,
2. patients \<18 years of age,
3. pregnant women,
4. heavy smokers, and
5. patients who underwent radiotherapy or chemotherapy are excluded.

Where this trial is running

Mahbūbnagar, Telangana

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Bone Regeneration
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.