Overview

Intracervical Block Versus Placebo to Assess Pain Control During Hysterosalpingogram

Status:
Completed
Trial end date:
2004-10-01
Target enrollment:
0
Participant gender:
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 2
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
59th Medical Wing
Wilford Hall Medical Center
Treatments:
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.