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A study to compare the numbness effect of 0.75% ropivacaine and 0.5% bupivacaine in surgical removal of wisdom tooth of lower jaw

A double blind randomized study to evaluate and compare the anaesthetic efficacy of 0.75% Ropivacaine and 0.5% Bupivacaine on the perioperative regional analgesia in impacted mandibular third molar surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023093
Enrollment
50
Registered
2020-02-03
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: Q899- Congenital malformation, unspecified

Interventions

Intervention1: Ropivacaine: Ropivacaine 0.75% Dose- 1.5- 2ml Frequency- Once Route of Administration- Intra-Oral Infiltration and Nerve Block Duration of anesthesia- 4-5 hours Control Intervention

Sponsors

Nisha Mishra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Impacted Mandibular 3rd molar

Exclusion criteria

Exclusion criteria: Allergic to any of the local anaesthetic solution Pregnant Women

Design outcomes

Primary

MeasureTime frame
Onset of Local Anaesthesthetic solution Timepoint: 15 minutes—

Secondary

MeasureTime frame
Duration of Local Anaesthetic solutionTimepoint: 1 hour—

Countries

India

Contacts

Public ContactDr Yogesh Sharma

Peoples Dental Academy

sharma.dryogesh@gmail.com9826048261

Outcome results

None listed

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