A randomized trial on evaluating the effects of multimodal pre-emptive analgesia in the patients undergoing transabdominal hysterectomy

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IPR-15005848

Enrollment

Unknown

Registered

2015-01-17

Start date

2014-02-05

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

multimodal pre-emptive analgesia

Interventions

1:control

2:P1

3:P2

4:P3

Eligibility

Sex/Gender

Female

Age

30 Years to 55 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria were physical status American Society of Anesthesiologists (ASA) I- II, aged between 30 and 55 years (mean age of 46.54±8.72), weighted between 50 and 75 kilogram (mean weight of 62.52±12.49 kg) undergoing transabdominal hysterectomy, and the operation time was between 55 and 80 min (mean time of 67.39±12.74 min).

Exclusion criteria

Exclusion criteria: Exclusion criteria were contraindication for epidural puncture, known allergy to local anesthetics, the patients with previous history of hypertension, diabetes, coronary heart disease or other medical history, the patients consumed opioids and non-steroidal anti-inflammatory drugs (NSAIDs) preoperatively, and patients with physiological and psychological disorders.

Design outcomes

Primary

Measure	Time frame
VAS;	—

Secondary

Measure	Time frame
Stress response;inflammatory cytokines;	—

Countries

China

Contacts

Public ContactJian-qing Chen

chenjianqing11@126.com+86 13606166881

Outcome results

None listed

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