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To evaluate whether pressure application helps make dental anesthesia injections less painful.

Assessing the effectiveness of pressure application on pain perception during local anesthetic administration. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097537
Enrollment
24
Registered
2025-11-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Health Condition 1: Z048- Encounter for examination and observation for other specified reasons

Interventions

Intervention1: Local Pressure application and Acupressure : Comparison of local pressure application versus acupressure, followed by local anesthetic administration, to assess pain perception during i

Sponsors

Dr Abhinaya Sathvika Kotagiri
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Children aged 6 to 9 years with written parental consent and child assent. 2. Children requiring bilateral greater palatine nerve block (GPNB) for dental procedures (e.g., Pulpectomy or extraction) in the upper arch. 3. Children with no previous history of dental local anesthesia injection. 4. Children exhibiting a cooperative behavior rated as Frankl s Behavior Rating Scale Grade III (Positive) or IV (Definitely Positive).

Exclusion criteria

Exclusion criteria: 1. Children with special health-care needs. 2. Children with a known allergy or hypersensitivity to local anaesthesia (specifically lignocaine or adrenaline). 3. Children with any cutaneous lesions (blisters, rashes, open wounds) or swelling on the dorsum of either hand near the Hegu (LI4) acupressure point. 4. Patients diagnosed with underlying vascular or significant hypersensitivity disorders.

Design outcomes

Primary

MeasureTime frame
Subjective Pain Perception was measured using the Wong Baker Faces Pain Rating Scale (WBS).Timepoint: before, during, after LA administration at 1 week, 2 weeks.

Secondary

MeasureTime frame
Objective Pain Perception was assessed using the Sound, Eye & Motor (SEM) scale.Timepoint: before, during, after LA administration at 1 week, 2 weeks.

Countries

India

Contacts

Public ContactDr Abhinaya Sathvika Kotagiri

Sibar Institute of Dental Sciences

kakarlapranitha@gmail.com9441818713

Outcome results

None listed

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