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Comparing the effect of Collacone and BoneProtect Cone in bone resorption

Comparison of the effect of Collacone and BoneProtect Cone in socket preservation: A triple-blind randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231105059969N1
Enrollment
45
Registered
2024-05-28
Start date
2024-05-30
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

socket preservation.

Interventions

Intervention 1: Control group:First, a medical history is taken from the patient and an oral examination is performed. Then, the conditions and purpose of the study will be explained to the patient, a

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Patient needs to extract a Maxillary anterior or premolar tooth. Patient must be between the ages of 18 and 45 without reported systemic disease and be in good general health and in the ASA I or ASA II group in terms of surgical risk. Patient should be in good oral health and without periodontal disease. Patient should not show any signs of lesion, acute inflammation and acute pain. The walls of the socket after tooth extraction should be intact and without noticeable fractures of the bone plates. All teeth must be atraumatically extracted with periotome, fine elevator and root forceps. Patient has accepted the conditions of the study after reading and signing the consent form.

Exclusion criteria

Exclusion criteria: Smokers Pregnant women Patients with a history of allergy to certain drugs or substances Patients who use drugs that interfere with bone healing process, such as bisphosphonates Patients with a history of radiotherapy or chemotherapy

Design outcomes

Primary

MeasureTime frame
Buccopalatal width of the alveolar ridge. Timepoint: Immediately after surgery and 90 days after surgery. Method of measurement: Cone-beam computed tomography (CBCT) radiology.;Height of bone. Timepoint: Immediately after surgery and 90 days after surgery. Method of measurement: Cone-beam computed tomography (CBCT) radiology.

Secondary

MeasureTime frame
Keratinized tissue width. Timepoint: Immediately after surgery and 90 days after surgery. Method of measurement: Periodontal probe.;Gum thickness. Timepoint: Immediately after surgery and 90 days after surgery. Method of measurement: Digital caliper and endodontic spreader.;Bone trabeculation. Timepoint: Immediately after surgery and 90 days after surgery. Method of measurement: cone-beam computed tomography radiology.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Hossein Moaddabi

Mazandaran University of Medical Sciences

a.moaddabi2@gmail.com+98 11 3324 4894

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026