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Effect of intravenous vitamin B12 in decreasing postoperative pain

Effect of intravenous vitamin B12 on postoperative analgesia-A prospective, randomized, double blind, controlled study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/07/034615
Enrollment
62
Registered
2021-07-06
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: C509- Malignant neoplasm of breast of unspecified site

Interventions

Intervention1: Effect of intravenous vitamin B12 on postoperative analgesia: Intravenous vitamin B12 1000micrograms in 100ml normal saline over 30minutes will be administered before induction of anaes

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Female patients aged 18 to 65 years scheduled for modified radical mastectomy under general anaesthesia. 2. Patients of American Society of Anesthesiologists(ASA) physical status I,II,III

Exclusion criteria

Exclusion criteria: 1.Patients with hepatic, renal, cardiac, endocrine, psychiatric and neurological disorders. 2. Patients with history of allergy to study drug. 3. Patients who received chemotherapy prior to surgery. 4. Patients with chronic pain syndrome on treatment with long term opioids. 5. Patients who cannot understand or interpret VAS for pain assessment. 6. Patients unwilling to participate in the study. 7. Patients unable to give informed consent. 8. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
1.Comparision of duration of analgesia between vitamin B12 group and control group 2. Comparision of total Tramadol consumption in 24hours postoperatively between vitamin b12 group and control groupTimepoint: Total Tramadol consumption in 24hours postoperatively.

Secondary

MeasureTime frame
1.To assess the magnitude of pain by Visual Analogue Scale(VAS) at different points of time. 2. To assess the sedation level using Ramsay sedation score 3. To observe adverse events during study period.Timepoint: T1-30minutes T2-1hour T3-2hours T4-4hours T5-6hours T6-24hours

Countries

India

Contacts

Public ContactDr P Hemalatha

SRI VENKATESWARA INSTITUTE OF MEDICAL SCIENCES

madhugastro@gmail.com9493547660

Outcome results

None listed

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