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Tramadol HCl as a local anaesthetic in exodontia.

Comparing the efficacy of TRAMADOL HCl with that of LIGNOCAINE HCl , as a local anaesthetic in supra periosteal infiltration for therapeuitic extraction of maxillary premolars: A SPLIT MOUTH STUDY.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026573
Enrollment
50
Registered
2020-07-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: R688- Other general symptoms and signs

Interventions

Control Intervention1: Inj. Tramadol HCl: Inj Tramadol HCL 2ml is compared with that of Lignocaine HCL in orthodontic extractions. 2mL of tramadol is diluted with sterile water in a ratio of 1:1. Tota

Sponsors

Dr Jinu Elizabeth James
Lead Sponsor
Dr Shashidhara Kamath K
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age :- 18-30 years of age of either sexes. 2. Patients having bilaterally indicated therapeutic extraction of maxillary premolars. 3. Patient with no history of allergy to drugs or anaesthetics used in the surgical protocol. 4. Patient who are willing to participate for the study

Exclusion criteria

Exclusion criteria: 1. Patients less than 18 years of age and above 30 years of age. 2. Patients with deleterious habits 3. Patients in whom extraction is medically contraindicated. 4. Patients with systemic diseases. 5. Patients with active local or systemic infection. 6. Patients on long term steroid therapy. 7. Patients with osseous pathology which may affect the surgical outcome and wound healing. 8. Patients with psychiatric disease or substance abuse. 9. Patients who are allergic to the drugs used for the surgical protocol. 10. Patients who have consumed analgesics within 6 hours prior to the surgical procedure. 11. Patients with Hb% less than 12gm/dL. 12. Pregnant and lactating women and those taking oral contraceptives. 13. Patients who are not willing for the study.

Design outcomes

Primary

MeasureTime frame
1.Pain scale during extraction of orthodontically indicated teeth, using VAS score. 2. Post operative analgesic effect after extraction of teeth.Timepoint: 1.Pain at the time of extraction of indicated teeth. 2. Post operative analgesic effect after extraction of teeth.—

Secondary

MeasureTime frame
Allergy to any of the drug to be assessed.Timepoint: Allergy occurring at the time of extraction or post operatively.—

Countries

India

Contacts

Public ContactDr Jinu Elizabeth James

Sri Hasanamba Dental College and Hospital

shashidhara.kamath@gmail.com6282421930

Outcome results

None listed

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