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Topical anesthesia in addition to intravaginal tablet misoprostol versus Paracervical block a form of anesthesia procedure for women undergoing Dilatation Curettage A Randomized controlled trail

Topial anesthesia in addition to intravaginal misoprostol versus Paracervical block for women undergoing Dilatation Curettage- A Randomized controlled trail

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/09/021465
Enrollment
128
Registered
2019-09-30
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: 4- Measurement and Monitoring

Interventions

Intervention1: Topical anesthesia in addition to intravaginal misoprostol versus Paracervical block for women undergoing Dilatation and curettage-A randomized controlled trail: comparing the VAS score

Sponsors

DeptOf Anesthesiology and Critical Care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: women undergoing Dilataion and Curettagein gynecological department

Exclusion criteria

Exclusion criteria: 1.cardiac disease 2.seziure disorder 3.bleeding disorder and patient on anticoagulant 4.asthma disease 5.patient on chronic glucocorticoid therapy 6.pregnancy

Design outcomes

Primary

MeasureTime frame
To compare the VAS score between topical anesthesia with intravaginal misoprostol and paracervical block for women undergoing dilataion and curettageTimepoint: VAS score was done during diatation and curettage

Secondary

MeasureTime frame
1.To compare the ambulation time and discharge time of the patients between the two techniques 2.To evaluate complications if any associated with misoprostol, lignocaine and paracervical block used for D&CTimepoint: 1.At baseline 2.During procedure 3.30 minutes after D&C;To compare the ambulation time and discharge time of the patients between the two techniques To evaluate complications if any associated with misoprostol lignocaine and paracervical block used for dilatation and curettageTimepoint: From starting of study to thirty minutes after dilataion and curettage

Countries

India

Contacts

Public ContactDr KARTHICK G

JIPMER

p_kundra@hotmail.com9367602030

Outcome results

None listed

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