study of the effects of two forms of epidural bupivacaine on postoperative pain following total knee replacement

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201502001010803

Enrollment

100

Registered

2015-01-25

Start date

2015-03-09

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Surgery postoperative pain

Interventions

heavy group

plain group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: ASA 2 and 3 patients who will undergo one side total knee replacement age from 50 to 80 , both male and female

Exclusion criteria

Exclusion criteria: ASA 4 patients patients who are receiving anti platelets till the operation day. patients with coagulopathies patients with sever back deformities or infection at the planned site of epidural hemodynamically unstable patients with poor systolic function.

Design outcomes

Primary

Measure	Time frame
pain score visual analogue 10 point score;first request for analgesia	—

Secondary

Measure	Time frame
sensory block onset and duration will be assessed by pin prick;motor block onset and duration	—

Countries

Egypt

Contacts

Public ContactMagdy chehata

lecturer of anesthesia ain shams university

magdychehata@yahoo.com00966563386721

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026