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A study comparing the effects of two methods of administration of nonsteroidal anti-inflammatory drugs (ibuprofen) combined with intravenous self-controlled analgesia on maternal analgesia and lactation after cesarean delivery

A study comparing the effects of two methods of administration of nonsteroidal anti-inflammatory drugs (ibuprofen) combined with intravenous self-controlled analgesia on maternal analgesia and lactation after cesarean delivery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082474
Enrollment
Unknown
Registered
2024-03-29
Start date
2022-08-15
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

cesarean section pain

Interventions

regular:In this group, NSAIDs (ibuprofen) 100 mg orally were given regularly starting 6 h after cesarean section, every 6 h until 42 h postoperatively.
on-demond:When a woman delivering by cesarean section feels pain after delivery and complains of wanting to take a nonsteroidal anti-inflammatory drug (ibuprofen), give ibuprofen 100 mg orally, and do

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: ? those whose mode of delivery was cesarean section; ? The American College of Anesthesiologists (ASA) is graded at the I-level; ? Patients who received intravenous disposable analgesic pumps after surgery; and ? those who gave informed consent.

Exclusion criteria

Exclusion criteria: (1) non-intravenous disposable analgesic pump users after cesarean section; (2) people with severe liver and kidney dysfunction; (3) people who need to undergo surgical procedures other than cesarean section; (4) people who need to be bed-rested or users of sedative medications after surgery; (5) people with history of psychiatric diseases; (6) people who are allergic to the medications used in this study.

Design outcomes

Primary

MeasureTime frame
pain score;Post-operative recovery;

Secondary

MeasureTime frame
satisfaction score;depression score;fatigue score;The initiation time of lactation;Exclusive breastfeeding rate;First bedtime activity time;postpartum exhaust time;

Countries

China

Contacts

Public ContactLiu Zhe

Peking University First Hospital

06067@pkufh.com+86 185 1003 1188

Outcome results

None listed

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