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Traditional versus vaginoscopic hysteroscopy,A Diagnostic tool in gynaecological problems in a tertiary care centre of kumaon - a comparative study

TRADITIONAL VERSUS VAGINOSCOPIC HYSTEROSCOPY, A DIAGNOSTIC TOOL IN GYNAECOLOGICAL PROBLEMS IN A TERTIARY CARE CENTRE OF KUMAON-A COMPARATIVE STUDY

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/052132
Enrollment
75
Registered
2023-04-28
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecified Health Condition 2: N850- Endometrial hyperplasia Health Condition 3: N921- Excessive and frequent menstruation with irregular cycle Health Condition 4: N920- Excessive and frequent menstruation with regular cycle Health Condition 5: N924- Excessive bleeding in the premenopausal period Health Condition 6: N971- Female infertility of tubal origin Health Condition 7: N972- Female infertility of uterine origin Health Condi

Interventions

Intervention1: Hysteroscope is being used by traditional approach.: In tradtional hysterscopy vulsellum is being used to grip cervix and then hysteroscope is introduced. Intervention2: Hysteroscopy do

Sponsors

Dr Shivani Pal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.All patients who are willing for study 2.All patients of infertility 3.Abnormal uterine bleeding (AUB) 4.Postmenopausal bleeding 5.Increased endometrial thickness in ultrasound, 6. Suspect of endometrial polyp, myoma or carcinoma, endocervical polyp 7.Recurrent pregnancy losses 8.Other gynecological complaints in which hysteroscopy is indicated.

Exclusion criteria

Exclusion criteria: 1.Patients who are not willing for study 2.Pregnant women 3.Cancer of the cervix 4.Active infection of the genital tract

Design outcomes

Primary

MeasureTime frame
Pain during intraoperative and postoperative period in both groups. Procedure time in both groups.Timepoint: 18 MONTHS

Secondary

MeasureTime frame
Intraoperative complications in both groups.Timepoint: 18 months

Countries

India

Contacts

Public ContactDr Shivani Pal

Government Medical College Haldwani

ikneiv@hotmail.com9412905449

Outcome results

None listed

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