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EVALUATION OF PAIN ASSESSMENT USING A NEUROMODULATION DEVICE AFTER SEPARATOR PLACEMENT: AN IN-VIVO STUDY

EVALUATION OF PAIN ASSESSMENT USING A NEUROMODULATION DEVICE AFTER SEPARATOR PLACEMENT: AN IN-VIVO STUDY - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078537
Enrollment
21
Registered
2024-12-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: U07- Health Condition 2: 8- Other Procedures

Interventions

Intervention1: NIL: NIL

Sponsors

Rahul Yadav
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with completely erupted upper first and second molars and compact interproximal contact areas on both upper first molars with healthy periodontal conditions1. 2. Patients with good oral health. 3. Patients ranging from the age of 12 to 24 years are selected for the study.

Exclusion criteria

Exclusion criteria: 1. Pregnant patients. 2. Patients with the history of seizures, cardiac arrythmia or pacemaker treatment. 3. Patients who were taking any over the counter or prescription pain medication during the testing period. 4. Interproximal caries or restoration 5. Extracted or missing teeth 6. Periodontally compromised teeth 7. Orofacial pain

Design outcomes

Primary

MeasureTime frame
Pain Perception and Assessment Using Wong Baker And Numeric Rating ScaleTimepoint: 2 Days—

Secondary

MeasureTime frame
Pain Perception Is Minimum In Experimental GroupTimepoint: 2 Days—

Countries

India

Contacts

Public ContactRAHUL YADAV

SUDHA RUSTAGI COLLEGE OF DENTAL SCIENCE AND RESEARCH

drrahulyadav420@gmail.com9654339744

Outcome results

None listed

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