Skip to content

Effects of transabdominal plane block for postoperative pain control of hysterectomy

A survey on analgesic effects of ultrasonographic transabdominal plane block for postoperative pain control of abdominal hysterectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013021012151N1
Enrollment
64
Registered
2013-03-10
Start date
2013-02-28
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Analgesic effect of trans abdominal block on post abdominal hysterectomy pain. Other procedures for purposes other than remedying health state

Interventions

Intervention 1: Intervention group: we use trans abdominal block with pain poump for post abdominal hysterectomy pain control. Intervention 2: control group : only using pain pump for control of after
Intervention group: we use trans abdominal block with pain poump for post abdominal hysterectomy pain control
control group : only using pain pump for control of after operation pain

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All of elective abdominal hysterectomies with pfanenstiel incision will enter to our study. Exclusion criteria: If the patient doesn’t accept; local anesthetic drugs allergy; infection on injection site; coagulation disorders; medical disorders that interfere with interpretation of pain; addiction to elicit drugs or alcohol; liver or renal insufficiency; sever obesity.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of post operation pain. Timepoint: 2 and 6 and 12 and 24 and 48 hours after operation. Method of measurement: Visual Analogue Scale test.

Secondary

MeasureTime frame
Amount of patient's satissfaction from after operation analgesia. Timepoint: 2 and 6 and 12 and 24 and 48 hours after operation. Method of measurement: Global Clinical Improvement (GCI) Test.;The amount of Fantanyle that will be used for pain pump. Timepoint: 2 and 6 and 12 and 24 and 48 hours after operation. Method of measurement: Micro geram of fantanyle that will be necessery for pain pump.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Fariba Almassinokiani ; Dr Farnad Imani

Tehran University of Medical Sciences

f-almasi@sina.tums.ac.ir+98 21 6650 9283

Outcome results

None listed

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