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Evaluating the efficacy of homoeopthic medicine Terebinthinae Oleum 30CH in treating urinary tract infection among teens and early adults: randomized control trial

Randomized Double Blinded Placebo Controlled Trial On Homoeopathic Medicine Terebinthinae Oleum 30 CH In The Management Of Acute Lower Urinary Tract Infection Among Teens And Early Adults - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/058041
Enrollment
60
Registered
2023-09-26
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: N390- Urinary tract infection, site notspecified

Interventions

Intervention1: Terebinthinae Oleum 30 CH: The study included a seven-day treatment period with Terebinthinae Oleum 30 CH and a 30-day follow-up period. Minimum of Four (4) visits were planned Contro

Sponsors

Sibin R A
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Clinical signs with one or more symptoms of a UTI. Onset of symptoms < 24 hours prior to study entry

Exclusion criteria

Exclusion criteria: Three or more episodes of acute UTI in the past 12 months; Known structural Genito-urinary abnormality patients Patients with evidence of factors like calculi, stricture, primary renal disease (e.g., polycystic renal disease), or neurogenic bladder; Patients with significant impaired immunity secondary to chemotherapy, oral corticosteroids. Patients with onset of symptoms > 24 hours prior to entry. Patients with temperature â�¥ 103�°F. Patients who received treatment with other antimicrobials within 48 hours prior to enrollment. Any significant medical or psychiatric condition that would render examination difficult or invalid or prevent the subject from active study participation. Patients under other medications or concomitant therapies which interfere the study

Design outcomes

Primary

MeasureTime frame
Analysis of Microbiological response during the therapeutic interventionTimepoint: three to seven days

Secondary

MeasureTime frame
Analysis of microbiological outcome per participant involved in the studyTimepoint: seven to thirty seven days

Countries

India

Contacts

Public ContactSibin R A

Sarada Krishna Homoeopathic Medical College and Hospital

sibinra1@gmail.com8848035605

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 27, 2026