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Pruritus Induced by Neuraxial Morphine After Cesarean Section: A Multicenter Prospective Observational Study

Pruritus Induced by Neuraxial Morphine After Cesarean Section: A Multicenter Prospective Observational Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-17012345
Enrollment
Unknown
Registered
2017-08-12
Start date
2017-08-11
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

Pruritus

Interventions

Case series:Neuraxial Morphine After Cesarean Section

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Receiving elective Cesarean section and epidural morphine analgesia; 2. Aged from 18 to 40 years; 3. Weight from 40 to 90 kg; 4. ASA I-II; 5. Intravertebral anesthesia.

Exclusion criteria

Exclusion criteria: 1. Pruritus-associated diseases: Cholestasis, hepatitis, cirrhosis, uremia, diabetes, malignany, neuropsychiatric diseases; 2. Severe hypertension, hepatic and renal disfunction; 3. Contraindication of intravertebral anesthesia.

Design outcomes

Primary

MeasureTime frame
Pruritus Intensity;—

Secondary

MeasureTime frame
Pain Intensity;—

Countries

China

Contacts

Public ContactShen Le

Peking Union Medical College Hospital

shenle@pumch.cn+86 010-69152024

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 20, 2026