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Homeopathic medicines for wisdom teeth

Efficacy of Cheiranthus cheiri 30CH in treatment of pericoronitis: A double-blind, randomized, placebo-controlled pilot trial by using pain visual analogue scale

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/051254
Enrollment
60
Registered
2023-04-03
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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: Cheiranthus cheiri 30CH, 4 doses a day for 3 days with concomitant care: Intervention is planned as administering Cheiranthus cheiri 30CH, 4 doses a day for 3 days. Each dose will consi

Sponsors

D. N. De Homoeopathic Medical College & Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age between 16 and 40 years. 2. Participants of either sex. 3. Patients having no history of tooth extraction/ exfoliation. 4. No filling for wisdom teeth or the second molar been undertaken before the study. 5. Providing with written informed consent voluntarily to participate in the study

Exclusion criteria

Exclusion criteria: 1. Incomplete root formation of the third molar 2. Craniofacial anomalies such as achondroplasia, progeria, oxycephaly, cleidocranial dysostosis 3. Down syndrome 4. Previous trauma or pathology 5. Pregnancy, puerperium, lactation 6. Vulnerable population – unconscious, non-ambulatory, too sick for consultation, differently abled, terminally or critically ill patients, mentally incompetent people 7. Diagnosed cases of unstable mental or psychiatric illness or other uncontrolled or life-threatening illness affecting quality of life or any organ failure. 8. Self-reported immune-compromised state 9. Substance abuse and/or dependence 10. Already undergoing homeopathic treatment for chronic disease within last 3 months 11. Simultaneous participation in any other clinical trial

Design outcomes

Primary

MeasureTime frame
Pain intensity measuring 0-100 mm visual analogue scaleTimepoint: Day 0, 3, 5, 7, 10, and 14

Secondary

MeasureTime frame
Blood ESR, CRP, and TLCTimepoint: Baseline and after 14 days;Oral Health Impact Profile 14 (OHIP-14) questionnaireTimepoint: Baseline and after 14 days;Swelling and trismusTimepoint: Day 0, 3, 5, 7, 10, and 14

Countries

India

Contacts

Public ContactAritra Roy Chowdhury

D. N. De Homoeopathic Medical College and Hospital

chandra.suman188@gmail.com9871630660

Outcome results

None listed

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