to prolong the spinal anesthesia and duration of analgesia by adminstrating epidural injection of two differant drugs and comparision

comparision of effect of additional epidural Neostigmine with epidural Magnesium sulfate on characteristics of spinal anesthesia in patients undergoing elective infraumbilical surgeries - a randomized, double blinded comparative study.

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/06/033984

Enrollment

Registered

2021-06-04

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: - Health Condition 2: O- Medical and Surgical

Interventions

Control Intervention1: inj. Neostigmine: to compare the charactaristics of spinal anesthesia after single shot epidural administration of inj. Neostigmine 100 micrograms in terms of sensory and motor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status grades I, II, III who are undergoing elective infraumbelical surgeries under spinal anesthesia

Exclusion criteria

Exclusion criteria: Pregnant and lactating women, morbidly obese, patients in whoom spinal anesthesia is contraindicated, allergic to study drugs, patients refusal to participate

Design outcomes

Secondary

Measure	Time frame
prolongation of duration of analgesiaTimepoint: post operative pain, sedation, patient satisfaction using visual analogue scale at 30min, 1st, 2nd, 3rd, 4th, 5th and 6th hourly	—

Primary

Measure	Time frame
sensory block assesment to loss of sensation to cold at L1 after spinal anesthesiaTimepoint: onset of sensory block, time taken to reach the maximum height of the block, time taken for two segment regression from maximum height of block.	—

Countries

India

Contacts

Public ContactDr Janaki Subhadra Peyyety

Sri Venkateswara Institute of Medical Sciences

subhadrapeyyety@gmail.com9390483725

Outcome results

None listed

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