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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00298480
Other study ID # 230-04s
Secondary ID
Status Recruiting
Phase N/A
First received March 1, 2006
Last updated April 18, 2007
Start date February 2005
Est. completion date July 2007

Study information

Verified date April 2007
Source Memorial Health Services Research Council
Contact Charlotte A Clock, M.D.
Phone 714-456-5967
Email cclock@uci.edu
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Transvaginal ultrasound of the cervix has become a common tool to evaluate patients who are at risk for preterm delivery. A shortened cervical length has been associated with an increased risk of preterm delivery. Dynamic cervical change is visible shortening(>6mm) of the cervix seen during the ultrasound examination. Prior studies have shown that the presence of dynamic change in patients with a shortened cervical length(<3cm) is not independently predictive of preterm delivery. However, a subset of patients with normal initial cervical length(>3cm) and dynamic change did demonstrate an increased rate of preterm delivery. Because this was a small sub-group, the present study was designed to obtain a larger sample size for further evaluation. The second focus of this study involves patients with a dilated cervix and whether cervical length adds predictive value to gestational age at delivery.

Patients presenting to with symptomatic preterm labor(vaginal pressure or uterine contractions), who consent to the study, will undergo the standard evaluation for preterm labor(described in detail below.) The only additional evaluation is a prolonged transvaginal ultrasound of approximately 10 minutes to evaluate for the presence of dynamic change during a contraction.

Null hypothesis:

Symptomatic preterm labor patients, with normal initial cervical length(>3cm), who exhibit dynamic cervical change deliver at a gestational age equal to those without dynamic change.

Alternative hypothesis:

Symptomatic preterm labor patients, with normal initial cervical length(>3cm), who exhibit dynamic cervical change deliver at an earlier gestational age than those without dynamic change.


Recruitment information / eligibility

Status Recruiting
Enrollment 220
Est. completion date July 2007
Est. primary completion date
Accepts healthy volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Pregnant women between the ages of 18 and 45 years.

- Intrauterine pregnancy with gestational age between 22 0/7 and 34 6/7 weeks gestation.

- Presenting with symptomatic preterm labor (e.g. Regular uterine contractions, uterine cramping, or pelvic pressure).

Exclusion Criteria:

- Cervical cerclage

- Ruptured membranes noted on initial speculum examination

- Cervical os dilation >4 cm noted on initial digital examination

- Known HIV-positive or active HSV(to minimize the risk of perinatal exposure)

- Presence of multiple genital warts

- Patients under extreme duress from their uterine contractions

Study Design

Observational Model: Case Control, Time Perspective: Longitudinal


Related Conditions & MeSH terms


Locations

Country Name City State
United States Saddleback Memorial Medical Center Laguna Hills California
United States Long Beach Memorial Medical Center Long Beach California
United States University of California, Irvine Medical Center Orange California

Sponsors (1)

Lead Sponsor Collaborator
Memorial Health Services Research Council

Country where clinical trial is conducted

United States,