Overview
Intracervical Block Versus Placebo to Assess Pain Control During Hysterosalpingogram
Status:
Completed
Completed
Trial end date:
2004-10-01
2004-10-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The purpose of this study is to compare the efficacy of 1% lidocaine intracervical block to placebo for pain control during the performance of a hysterosalpingogram (HSG). We hypothesized that an intracervical block would decrease pain during a hysterosalpingogram.Phase:
Phase 2Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
59th Medical Wing
Wilford Hall Medical CenterTreatments:
Lidocaine
Criteria
Inclusion Criteria:- All patients without a known cause for their infertility who were undergoing a
hysterosalpingogram were eligible for enrollment.
- All subjects were 18 to 40 years of age and married.
Exclusion Criteria:
- Included a history of any allergies to local anesthetics, radio-opaque dye or to
anti-inflammatory medications.