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A quality assurance exercise to assess the efficacy of oral multimodal analgesic regime for acute pain control after caesarian section

A quality assurance exercise to assess the efficacy of oral multimodal analgesic regime for acute pain control after caesarian section

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052057
Enrollment
Unknown
Registered
2021-10-15
Start date
2021-10-18
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Analgesia after cesarean section

Interventions

Combined analgesia group:No

Sponsors

The University of Hong Kong - Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Post-cesarean parturients who had received the combination of oral paracetamol, diclofenac and tramadol for postoperative analgesia.

Exclusion criteria

Exclusion criteria: Pregnant women who contraindicate to tramadol, paracetamol and diclofenac sodium.

Design outcomes

Primary

MeasureTime frame
NRS with movement;NRS (Numerical Rating Scale) at rest;—

Secondary

MeasureTime frame
The proportion of people experiencing side effects of analgesics;The proportion of people receiving acute pain relief treatment with oxycodone or morphine;—

Countries

China

Contacts

Public ContactYu Yang

The University of Hong Kong - Shenzhen Hospital

yuy8@hku-szh.org+86 15099906805

Outcome results

None listed

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