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Effect of intravenous analgesia after cesarean section with lidocaine: a randomized controlled trial.

Effect of intravenous analgesia after cesarean section with lidocaine: a randomized controlled trial.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053253
Enrollment
Unknown
Registered
2021-11-17
Start date
2021-11-30
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Cesarean section

Interventions

Sponsors

Maternal and Child Health Hospital of Anhui Province
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Subjects undergoing cesarean section; 2. ASA grade I-II; 3. Aged 25-35 years; 4. Weight 65-90 kg, height 160-170 cm.

Exclusion criteria

Exclusion criteria: 1. MMSE score < 24; 2. Patients with abnormal heart, lung, liver and kidney function; 3. Maternal women have complications during pregnancy, nervous system diseases and contraindications in spinal canal; 4. Patients with severe visual or hearing impairment; 5. Long-term use of sedatives or antidepressants, history of alcoholism.

Design outcomes

Primary

MeasureTime frame
VAS(Visual Analogue Scale) score;Times of manual pressure of analgesic pump;

Secondary

MeasureTime frame
First flatus;First bowel movement;Number of hospital days;Postoperative nausea and vomiting;

Countries

China

Contacts

Public ContactWang Pei

Maternal and Child Health Hospital of Anhui Province

827740295@qq.com+86 13957712366

Outcome results

None listed

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