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A clinical trial to compare and evaluate the stability of dental implants placed using two techniques, conventional drill and magnetic mallet.

Comparative evaluation of stability of dental implants placed using conventional drill versus magnetic mallet - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/066806
Enrollment
20
Registered
2024-05-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: K084- Partial loss of teeth

Interventions

Intervention1: Magnetic mallet technique: Dental implants will be placed using magnetic malleting technique. Duration of intervention- 24 months Control Intervention1: Conventional drill technique: De

Sponsors

Yangchan Dolma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects of either sex between the age group of 20 to 55 years who sign the informed consent for the study. 2. Presence of single or multiple edentulous areas in maxilla and/or mandible. 3. Subjects who want dental implant and have sufficient available bone for implant placement. 4. Subjects having sound general health. 5. Absence of any signs of pathology at surgical site. 6. Non-smokers

Exclusion criteria

Exclusion criteria: 1. Presence of poor oral hygiene. 2. Uncontrolled systemic diseases (e.g., uncontrolled diabetes, uncontrolled hypertension, bleeding disorders), on immunosuppressive or anti-coagulation medications. 3. Presence of acute or chronic sinus problems. 4. Presence of bone disease (Paget disease, rickets, osteoporosis, arthritis, multiple myeloma etc.). And radiographic evidence of bone tumor (benign/malignant) or cyst. 5. Subjects under long-term bisphosphonate therapy. 6. Pregnant women and/or expected pregnancy during the study period. 7. Lactating women. 8. Alcohol or drug abuse.

Design outcomes

Secondary

MeasureTime frame
Patient centered outcome- discomfort experienced during the surgical procedure.Timepoint: on the day of dental implant placement

Primary

MeasureTime frame
Implant stabilityTimepoint: immediately after dental implant placement and at 6 months

Countries

India

Contacts

Public ContactYangchan Dolma

Maulana Azad Institute of Dental Sciences

arundeep.kaur.lamba@gmail.com9654700980

Outcome results

None listed

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