MedPath

A comparative assessment on the effectiveness of paracervical block and rectal diclofenac for pain relief during diagnostic hysteroscopy.

Phase 2
Not yet recruiting
Conditions
No
Registration Number
PACTR202303663072593
Lead Sponsor
Duru Victor Chinazom
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
100
Inclusion Criteria

?Women undergoing diagnostic hysteroscopy and gave consent for the study

Exclusion Criteria

1.Women who are allergic to lignocaine/diclofenac
2.Women who had failed attempts at previous hysteroscopy
3.Women with cervicitis or active pelvic inflammatory disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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