To compare the effectiveness of intravenous magnesium sulphate and paracetamol in reducing the pain after surgery in patients undergoing Total abdominal hysterectomy

A comparison of post operative analgesia of magnesium sulphate to paracetamol intravenously in patients undergoing total abdominal hysterectomy under subarachnoid block in tertiary care center in kerala - nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/07/055582

Enrollment

Registered

2023-07-24

Start date

Unknown

Completion date

Unknown

Last updated

2023-08-21

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

Conditions

Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecified Health Condition 2: N926- Irregular menstruation, unspecified

Interventions

Intervention1: Comparing the post operative analgesic effect of intravenous Magnesium sulphate and Paracetamol in patients undergoing total abdominal hysterectomy under Sub arachnoid block: patients a

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA grade 1 and 2 patients

Exclusion criteria

Exclusion criteria: 1.Emergency surgeries 2.BMI > 40kg/m2 3.Patients with known allergy to the drugs used in study 4.Patients with renal insufficiency 5.Neuromuscular diseases 6.Hepatic dysfunction 7.Cardiac disease 8.Previous oncological surgery

Design outcomes

Primary

Measure	Time frame
Pain score in both the groupTimepoint: 0hr, 4hr, 8 hr, 12hr , 16hr, 20 hr , 24hr	—

Secondary

Measure	Time frame
â?¢Total analgesic requirement in the two groups in first 24 hours â?¢Time (in minutes) to request first analgesic in both groups â?¢Frequency of occurrence of side-effects of magnesium sulphateTimepoint: 0 hour, 4 hours, 8 hours , 12 hours , 16 hours, 20 hours, 24 hours	—

Countries

India

Contacts

Public ContactANU ELSA BOBBY

pushpagiri medical college and research centre thiruvalla

mathewskthomas@yahoo.com7356879388

Outcome results

None listed

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