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efficacy of lignocaine in distension medium to reduce pain perceived during office hysteroscopy

Not Applicable
Registration Number
CTRI/2023/03/051204
Lead Sponsor
INSTITUTE,AIIMS NEW DELHI
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.All women aged 20-55 years undergoing office hysteroscopy(AUB, Infertility, Recurrent pregnancy loss etc.)

2.willing to participate and sign informed written consent

3.participants falling in ASA I&II

Exclusion Criteria

1.Those requiring operative intervention

2.Acute Pelvic Inflammatory Disease(PID)

3.Known cervical malignancy

4.Active bleeding

5.Marked cervical stenosis/Previous cervical surgery

6.Women with neurological disorders affecting evaluation of pain

7.women with h/o AV Block, sick sinus syndrome and underlying heart procedure

8.women allergic to lignocaine

Study & Design

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