Comparative Study between Epidural analgesia Versus subcutaneous nalbuphen For Postoperative Analgesia After Abdominal Surgeries.

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

PACTR

Registry ID

PACTR202001875909224

Enrollment

130

Registered

2020-01-13

Start date

2019-12-19

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Anaesthesia

Interventions

epidural analgesia

subcutaneous nalbuphen

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: the American Society of Anesthesiologists physical status class I and II undergoing elective surgeries

Exclusion criteria

Exclusion criteria: physical dependence to opioids; hepatic and renal disease; who were pregnant and lactating, elderly, diabetes, asthma, epilepsy, bleeding disorder, receiving central nervous system depressants, established respiratory depression; a history of hypersensitivity to study drugs; not willing to participate in the study

Design outcomes

Primary

Measure	Time frame
the time of first call of analgesia	—

Secondary

Measure	Time frame
The amount of analgesics used in the first 24 postoperative hours, Intraoperative need of analgesics,VAS , all the patients were also evaluated for any complications and their satisfaction	—

Countries

Egypt

Contacts

Public Contactnoha afify

lecturer of anesthesia and intensive care

nohaafify2014@gmail.com01069113014

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026