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Comparison of anesthesia effectiveness and safety of 0.5% Levobupivacaine and 0.5% Ropivacaine in inferior alveolar nerve block among patients undergoing lower impacted wisdom tooth removal.

Comparative evaluation of Anesthetic potency of 0.5% Levobupivacaine and 0.5% Ropivacaine in inferior alveolar nerve block among patients undergoing lower impacted third molar surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/059014
Enrollment
60
Registered
2023-10-23
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Health Condition 1: K011- Impacted teeth

Interventions

Intervention1: LOCAL ANESTHESIA DURING THIRD MOLAR SURGERY.: To compare and evaluate the latency, pain threshold, duration of post operative analgesia, time to rescue analgesia, total analgesic requir

Sponsors

SHARAD PAWAR DENTAL COLLEGE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Individuals with ASA Gr I status 2. Individuals between 18 to 40 years 3. Presence of at least one asymptomatic impacted mandibular third molar having moderately difficult score Class II Position B.

Exclusion criteria

Exclusion criteria: 1. Patient who has history of drug dependence. 2. Patients with systemic disease such as HTN, DM, blood dyscrasias, immunocompromised status. 3. Patients who is chronic smoker. 4. Patients with allergy to local anesthetic agents used in the study. 5. Patients who is Pregnant and nursing mother. 6. Females who are on oral contraceptives. 7. Patients undergoing treatment with antibiotics and anti-inflammatory drugs. 8. Patient showing signs of any local infection like pericoronitis/pterygomandibular space infection. 9. Patient who shows presence of any chronic facial pain on the side of administration. 10. Patient whose radiograph shows Inferior alveolar canal approximation. 11. Patients who have any psychiatric illness

Design outcomes

Primary

MeasureTime frame
1)Pain threshold2) Duration of postoperative analgesia 3) Time to rescue analgesic 4)Adverse effects Timepoint: 1)WITHIN 24 HOURS 2)WITHIN 24 HOURS 3) WITHIN 24 HOURS 4)WITHIN 24 HOURS

Secondary

MeasureTime frame
1)Latency of anesthesia 2)Total analgesic requirements 3) Mean VAS scoreTimepoint: TOTAL 24 HOURS

Countries

India

Contacts

Public ContactSUROLIA PRACHI SATYAPRAKASH

PROFESSOR

rajanikanthmalaviya@gmail.com

Outcome results

None listed

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