COMPARISON OF HYPERBARIC ROPIVACAINE, HYPERBARIC ROPIVACAINE WITH MAGNESIUM SULFATE AND HYPERBARIC ROPIVACAINE WITH DEXMEDETOMIDINE IN BELOW UMBILICAL SURGERIES UNDER SPINAL ANAESTHESIA IN TERMS OF DURATION OF MOTOR AND SENSORY BLOCKADE.

COMPARISON OF HYPERBARIC ROPIVACAINE,HYPERBARIC ROPIVACAINE WITH MAGNESIUM SULFATE AND HYPERBARIC ROPIVACAINE WITH DEXMEDETOMIDINE IN INFRA-UMBILICAL SURGERIES UNDER SUB- ARACHNOID BLOCK (SAB) IN TERMS OF DURATION OF MOTOR AND SENSORY BLOCKADE: A SINGLE Ã¢â?¬â?? BLIND RANDOMIZED CLINICAL TRIAL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/09/045572

Enrollment

Registered

2022-09-15

Start date

Unknown

Completion date

Unknown

Last updated

2022-10-17

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

Conditions

Health Condition 1: K402- Bilateral inguinal hernia, withoutobstruction or gangrene Health Condition 2: N210- Calculus in bladder Health Condition 3: N211- Calculus in urethra Health Condition 4: N40-N53- Diseases of male genital organs Health Condition 5: N70-N77- Inflammatory diseases of female pelvic organs Health Condition 6: S90-S99- Injuries to the ankle and foot Health Condition 7: S70-S79- Injuries to the hip and thigh Health Condition 8: S80-S89- Injuries to the knee and lower le

Interventions

Intervention1: comparision of hyperbaric ropivacaine 0.75% , hyperbaric ropivacaine with magnesium sulphate 75mg , hyperbaric ropivacaine with dexmedetomidine 10 microgram in infraumbilical surgeries

Eligibility

Inclusion criteria

Inclusion criteria: Patient of ASA grade 1 and 2, BMI 20-35kg/m2 , who has given valid written informed consent for infra umbilical elective surgeries under spinal anaesthesia .

Exclusion criteria

Exclusion criteria: Patient Refusal,Lack Of Informed Written Consent, Coagulopathy, Spinal deformity, infection At The Injection Site, ASA grade 3 and 4, Allergic Reaction to Local Anaesthetic Drugs And Adjuvants, on Anticoagulants, History of Seizure And Neurological Deficit, Pregnant Females, Severe Hepatic/Renal/Respiratory/Cardiovascular Disease, Surgeries Started With Subarachnoid Block But Converted to General Anaesthesia in Between It Will be Exempted From The Sudy.

Design outcomes

Primary

Measure	Time frame
comparision of total duration of motor and sensory block in infraumbilical surgeries under subarachnoid block in all three study groups.Timepoint: block level noted after intrathecal injection at 2 min. interval upto 15 min. than 5 min. interval upto 30 mun. than 15 min. interval upto 120 min. than postoperatively at 2,4,6 hrs.	—

Secondary

Measure	Time frame
comparision of time of onset of motor and sensory block, time to achieve T10 level sensory block, time to achieve T6 level sensory block , time to achieve complete motor block, comparision of perioperative hemodynamic changes, any side effect due to combination of drugs.Timepoint: all parameters noted after intrathecal injection at 2 min. interval upto 15 min. than 5 min. interval upto 30 min than 15 min. interval upto 120 min. than postoperatively at 2,4 and 6 hrs.	—

Measure

Time frame

comparision of time of onset of motor and sensory block, time to achieve T10 level sensory block, time to achieve T6 level sensory block , time to achieve complete motor block, comparision of perioperative hemodynamic changes, any side effect due to combination of drugs.Timepoint: all parameters noted after intrathecal injection at 2 min. interval upto 15 min. than 5 min. interval upto 30 min than 15 min. interval upto 120 min. than postoperatively at 2,4 and 6 hrs.

—

Countries

India

Contacts

Public ContactSher Singh

Dr SN Medical College Jodhpur Rajasthan

dr.rajendrasolanki51@gmail.com9414131931

Outcome results

None listed

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