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the effect of magnesium sulfate injection in surgical incision for postoperative pain control

The effect of magnesium sulfate local injection in surgical incision for cesarean section postoperative pain control

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201104303247N2
Enrollment
192
Registered
2011-05-19
Start date
2010-04-21
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

Acute postoperative pain. Acute pain

Interventions

Intervention 1: Intervention group: at the end of surgery and before closing the wound 20 ml mixture of 750 mg magnesium sulfate and normal saline is injected locally in the operation site. Interventi
Treatment - Drugs
Placebo
Intervention group: at the end of surgery and before closing the wound 20 ml mixture of 750 mg magnesium sulfate and normal saline is injected locally in the operation site
Control group: 20 ml of normal saline is injected

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: pregnant women with anesthetic class ASA1 or 2 and age range of 20 -35 years, no history of: pre eclampsia , chronic hypertension, heart, liver, kidney and mental disorders, chronic opioid abuse, calcium channel blocker medications, and elective operations. Exclusion criteria: If the anesthetic level is not satisfactory and we have to give opioids or anesthetics during surgery or if magnesium sulfate has to be given generally for hypertensive postoperative patients

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Postoperative pain intensity. Timepoint: 4, 8, 12 and 24 hours postoperatively. Method of measurement: Visual analog Scale.;Amount of diclofenac supposetories required. Timepoint: During first 24 hour postoperatively. Method of measurement: mg.;Amount of intramuscular pethidine required. Timepoint: 24 hours postoperatively. Method of measurement: Mili gram (mg).

Secondary

MeasureTime frame
Possible side effects. Timepoint: During the first 24 hour postoperatively. Method of measurement: Patients medical records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Shirin Pazoki

Arak University of Medical Sciences

pazooki.sh@arakmu.ac.ir+98 86 1277 6063

Outcome results

None listed

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