Comparison of Postoperative Pain Between Patients Received Primary and Repeated Caesarean Section

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03009955

Enrollment

168

Registered

2017-01-04

Start date

2016-12-31

Completion date

2017-06-30

Last updated

2017-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caesarean Section

Brief summary

To everyone knows, more and more patients received repeated caesarean section in China. However, at present it is not known what is it like about their postoperative pain intensity, and is it different from those patients who received primary caesarean section. Thus through postoperative follow-up, the current study aimed to investigate and compare the postoperative pain between patients received primary and repeated caesarean section.

Detailed description

According to whether or not to receive repeated caesarean patients were grouped into group P or group R. For all maternal,standardized epidural anesthesia and caesarean section were performed. Then the pain VAS scores and Ramsay scores at 4h, 8h, 12h, 24h and 48h after the surgery were recorded. And sleep quality at 1 day and 2 day after the surgery were recorded. In addition, pain situation at 1 week and 4 weeks after the surgery was followed up.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

20 Years to 40 Years

Healthy volunteers

Inclusion criteria

* single birth * full-term pregnancy * in accordance with cesarean section indications * transverse incision of lower uterine segment

Exclusion criteria

* history of dementia, psychiatric illness or any diseases of central nervous system * accompanying liver or kidney function deficiency * alcoholism and drug dependence * patients previously included in this study or currently included in the other clinical study * patients who have second surgery during the study period * difficult to follow up or patients with poor compliance * history of chronic pain

Design outcomes

Primary

Measure	Time frame
Pain VAS at 4, 8, 12, 24 and 48 hours after the surgery	At 4, 8, 12, 24 and 48 hours after the surgery

Secondary

Measure	Time frame
Pain intensity at 3 to 7 days after the surgery	At 3 to 7 days after the surgery
Pain intensity at 4 weeks after the surgery	At 4 weeks after the surgery

Countries

China

Outcome results