Pain score during endometrium biopsy procedure Endometrial biopsy paracervical block Lidocaine spray
Conditions
Interventions
first groups receive paracervical block with 1%lidocaine and 0.9%NSS spray(placebo),the second groups receive 10%lidocaine spray and paracervical block with 0.9%NSS(placebo),the third groups receive p
paracervical block with 1%lidocaine and 0.9%NSS spray(placebo),10%lidocaine spray and paracervical block with 0.9%NSS,receive placebo both paracervical block and spray
Sponsors
None listed
Eligibility
Sex/Gender
Female
Age
30 Years to 70 Years
Inclusion criteria
Inclusion criteria: The women age who had abnormal uterine bleeding and indication for endometrial biopsy were enrolled.
Exclusion criteria
Exclusion criteria: Exclusion Criteria: �1) contraindications to NSAID or Lidocaine - known sensitivity to these drugs; 2) pregnancy; 3) genital tract infection; 4) coagulation disorder; and 5) unstable vital signs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score during endometrium biopsy during and post endometrium biopsy 15 min Numerical Rating Scale(NRS) | — |
Secondary
| Measure | Time frame |
|---|---|
| to determine the adverse effects during and post endometrium biopsy such as dizziness, nausea, vomiting, pelvic pain, bleeding | — |
Countries
Thailand
Contacts
Public ContactAkarawit Jitchanwichai
Obstetric and gynecology department Songkla nakarin hospital
Outcome results
None listed