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Pain relief during uterine curettage procedure using 2 different methods. 1) injecting local anesthesia on either side of cervix. 2) spraying local anesthesia inside the uterine cavity.

Transcervical intrauterine lidocaine instillation v/s paracervical block for pain control during Dilation and Curettage: A prospective interventional study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/10/010186
Enrollment
100
Registered
2017-10-25
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patient suffering from abnormal uterine bleeding and those needing endometrial sampling

Interventions

Intervention1: lidocaine: Transcervical intrauterine lidocaine instillation v/s paracervical block for pain control during Dilation and Curettage. 2 group each of 50-1 group will receive paracervical

Sponsors

kasturba medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)All women with Abnormal uterine bleeding scheduled for dilation and curettage. 2)Women who need endometrial curettage prior to surgery

Exclusion criteria

Exclusion criteria: 1) Women allergic to lidocaine, 2) Profuse uterine bleeding , 3) Profuse white discharge , 4) Impaired liver functions, 5) Unable to understand VAS (visual analogue scale of 10)

Design outcomes

Primary

MeasureTime frame
Compare the effectiveness of lidocaine to that of commonly used paracervical block for pain management in dilation and curettage with visual analogue scale of 10.Timepoint: At time of procedure and 30 minutes post procedure.—

Secondary

MeasureTime frame
histopathalogical changes associated with the use of different anesthesiaTimepoint: 2 weeks after procedure—

Countries

India

Contacts

Public ContactSwati kanchan

kasturba medical college, Manipal

shripad.hebbar@manipal.edu9611786463

Outcome results

None listed

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