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Comparison of analgesic titer between regular oral non-steroidal anti-inflammatory drugs combined with acetaminophen and patient-controlled intravenous analgesia after elective cesarean section with a single lumbar anesthesia

Comparison of analgesic titer between regular oral non-steroidal anti-inflammatory drugs combined with acetaminophen and patient-controlled intravenous analgesia after elective cesarean section with a single lumbar anesthesia

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400093275
Enrollment
Unknown
Registered
2024-12-02
Start date
2025-01-01
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

analgesia after elective cesarean section

Interventions

Intravenous analgesic pumps group:None
Regular oral analgesics group :None

Sponsors

Beijing Jishuitan Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Without gestational hypertension; 2.Monocyesis ; 3.Elective cesarean section with single lumbar anesthesia.

Exclusion criteria

Exclusion criteria: 1. The anesthetic effect is unsatisfactory, additional drugs or changes to the anesthesia protocol will be administered; 2. More than 1,000 ml of blood loss during surgery; 3. Surgery lasts more than 2 hours; 4. Uterine fibroid surgery is performed during the procedure; 5. Cesarean section surgery with Placenta previa; 6. Vertical incision surgery; 7. History of gastrointestinal ulcer or contraindications to the use of nonsteroidal anti-inflammatory drugs or acetaminophen; 8. Patients who refuse to cooperate in filling out the ERAC observation form or fail to take medication as required.

Design outcomes

Primary

MeasureTime frame
VAS pain grade;

Secondary

MeasureTime frame
The rate of addition of opioid analgesics after surgery;Postoperative exhaust time;Incidence of postoperative urinary retention;

Countries

China

Contacts

Public ContactGong Kangzi

Beijing Jishuitan Hospital

gkz19911010@163.com+86 186 1238 9672

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026