Cold Compress Clinical Trial
Official title:
Effect of Perineal Massage Combined With Cold Compress in the Second Stage on the Delivery Outcome of Primipara
Verified date | April 2022 |
Source | Second Affiliated Hospital of Wenzhou Medical University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Objective: The aim of this study was to investigate the effect of perineal massage and cold compress in second stage on the delivery outcome of primipara. Method: This interventional study included a total of 200 primipara hoping for natural birth. Patients were randomly divided into two groups, one group used routine labor, one group used cold compress and perineal massage. Record the time of second stage of labor, degree of perineal laceration, etc.
Status | Not yet recruiting |
Enrollment | 200 |
Est. completion date | April 2024 |
Est. primary completion date | December 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 20 Years to 35 Years |
Eligibility | Inclusion Criteria: - want give birth naturally - have well developed perineum Exclusion Criteria: - Abnormal fetal position and head basin - Severe obstetric complications |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
---|---|
Second Affiliated Hospital of Wenzhou Medical University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | the time of second stage of labor | calculate the time taken for the second stage of labor | until the end of the second stage of labor | |
Primary | Degree of perineal laceration | The degree of perineal laceration was judged according to the degree of perineal division table | about 30 minutes after the pregnant woman gives birth | |
Primary | Lateral perineal resection rate | observe whether perineal lateral excision was performed during delivery | until the end of the second stage of labor | |
Primary | Hospitalization days | observe how long pregnant women stay in the hospital | up to 2 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02898831 -
Cold Compress for Pain Associated With Intrauterine Device Insertion
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N/A |