Health Condition 1: 4- Measurement and Monitoring
Conditions
Interventions
Sponsors
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
| Measure | Time 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
| Measure | Time 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
JIPMER