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A clinical study to asses effect of lajjalu oil tampons in cervical erosion.

A Randomized Controlled Clinical Trial to Evaluate the Effect of Lajjalu Siddha Taila Yonipichu in the Management of Garbhashaya Mukhagat Vrana with Special Reference to Cervical Erosion. - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100984
Enrollment
70
Registered
2026-01-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: N86- Erosion and ectropion of cervix uteri

Interventions

None listed

Sponsors

Vd Sheela Sambhaji Chavan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Women aged 19 to 50 years will be included in the study. 2 Married women will be selected irrespective of parity. 3 Presence of cervical erosion will be confirmed on per speculum examination. 4 Women presenting with signs and symptoms such as vaginal discharge, post-coital bleeding, low backache, and dyspareunia will be included.

Exclusion criteria

Exclusion criteria: 1 Women who are pregnant or in the postpartum period within 6 weeks will be excluded. 2 Patients currently using oral contraceptive pills will be excluded. 3 Known cases of cervical intraepithelial neoplasia or previously treated cervical carcinoma will be excluded. 4 Patients showing malignant changes on Pap smear examination will be excluded. 5 Patients who are HIV, HBsAg, or VDRL positive will be excluded. 6 Women with intrauterine contraceptive device insertion will be excluded. 7 Patients suffering from severe systemic disorders such as uncontrolled diabetes mellitus, tuberculosis, or hypertension will be excluded.

Design outcomes

Primary

MeasureTime frame
1 Reduction or disappearance of Nabothian cysts, if present. 2 Restoration of cervical tone and mucosal integrity. 3 Assessment of tolerance, safety, and patient acceptability of the procedure. 4 Improvement in per speculum findings.Timepoint: 1 week

Secondary

MeasureTime frame
1 Reduction or disappearance of Nabothian cysts, if present. 2 Restoration of cervical tone & mucosal integrity. 3 Assessment of tolerance, safety, & patient acceptability of the procedure. 4 Improvement in per speculum findings.Timepoint: 1 week

Countries

India

Contacts

Public ContactVd Manoj Vitthal Gaikwad

R A Podar Medical College (Ayu),Worli,Mumbai,400018.

drmanojvgaikwad@gmail.com9822752816

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026