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To reduce the pain while giving injection in mouth by comparing two techniques.

Acupressure vs topical gel as preanesthetic technique in children A split mouth study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068367
Enrollment
80
Registered
2024-06-05
Start date
Unknown
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

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Aculief Acupressure Device.: Aculief acupressure device attached to LI4 point to reduce pain in needle insertion during local anesthesia to be used in all the 80 cases over a period of

Sponsors

Dr Nidhi Chauhan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. children who require any pediatric procedure to be done under local anesthesia. 2. Children with no prior experience with local anesthesia. 3. Children with Frankl behavior rating scale grade 3 and 4.

Exclusion criteria

Exclusion criteria: 1. Children with special health care needs. 2. Patients with blisters, rashes, open wounds and swelling in and around LI 4 acupressure point. 3. Patients with history of hypersensitivity reactions to anesthetic agents. 4. Recent trauma to oral tissues.

Design outcomes

Primary

MeasureTime frame
The aim of the study is to evaluate the effect of the aculief acupressure device on the reduction of during local anesthesia in children and compare it with the topical anesthetic gel.Timepoint: After a period of 1 year.

Secondary

MeasureTime frame
1. To evaluate the effect of the Aculief acupressure device on the reduction of pain during LA in children using SEM scale & Wong-Bakers FACES Pain Rating scale. 2. To evaluate the effectiveness of topical anesthetic gel on needle insertion pain during administration of LA using SEM scale & Wong-Bakers FACES Pain Rating scale. 3. To compare & evaluate the effect of the Aculief acupressure device with topical gel during LA administration.Timepoint: Over a period of 1 year.

Countries

India

Contacts

Public ContactNidhi Chauhan

SGT University, Gurugram, Haryana.

anil.gupta@sgtuniversity.org9899039805

Outcome results

None listed

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