Comparison of Bupivacaine used alone with mixture of Bupivacaine and Lidocaine used for giving anaesthesia for cataract surgery

Effect of mixture of Bupivacaine and Lidocaine versus Bupivacaine alone with and without adrenaline, in Peribulbar blocks in Cataract surgeries - EBBL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/08/015541

Enrollment

Registered

2018-08-30

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: H250- Age-related incipient cataract Health Condition 2: H251- Age-related nuclear cataract

Interventions

Intervention1: Our study is a 4 arm study, the Intervension agent in our study is Bupivacaine 0.5% with adrenaline in the first group and Bupivacaine 0.5% without adrenaline in the second group. : In

Eligibility

Inclusion criteria

Inclusion criteria: 1. patients of age between 20 and 80 2. American Society of Anaesthesiologists (ASA) grade I and II 3. Both Male and Female 4. attending our tertiary care Medical College Hospital for elective cataract extraction and Intra ocular Lens Implantation surgery 5. up to a total of 80 numbers between the period from 15 August 2018 to 31st December 2018

Exclusion criteria

Exclusion criteria: 1. patients with known allergy to study drugs, 2. patient refusal of local anaesthetic block, 3. high myopia, glaucoma, 4. ocular infection, 5. mental retardation, 6. uncontrolled hypertension 7. chronic obstructive pulmonary disease (COPD).

Design outcomes

Primary

Measure	Time frame
1.measurement of duration of onset of block both motor and sensory 2.measurement of total duration of the block Timepoint: 1.measurement of duration of onset of block both motor and sensory 2.measurement of total duration of the block	—

Secondary

Measure	Time frame
1.Measuring Changes in heart rate mean arterial pressure 2.Measuring changes in Respiratory rate 3.Measuring changes in Saturaton of peripheral Oxygen 4.recording incidence of allergic reactions 5.Recording incidence of other adverse events like nausea vomiting , dryness of mouth 6.Assessing occurence of Pain or discomfort during surgery 7.measurement of Total analgesic requirement for the first 24 hours 8.assessment of Surgeon and patient satisfaction scores Timepoint: 1. every 5 min till the end of surgery 2. every 15 min while the patient remained in post anaesthesia care unit (PACU) for 2 hours.	—

Measure

Time frame

1.Measuring Changes in heart rate mean arterial pressure 2.Measuring changes in Respiratory rate 3.Measuring changes in Saturaton of peripheral Oxygen 4.recording incidence of allergic reactions 5.Recording incidence of other adverse events like nausea vomiting , dryness of mouth 6.Assessing occurence of Pain or discomfort during surgery 7.measurement of Total analgesic requirement for the first 24 hours 8.assessment of Surgeon and patient satisfaction scores Timepoint: 1. every 5 min till the end of surgery 2. every 15 min while the patient remained in post anaesthesia care unit (PACU) for 2 hours.

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Countries

India

Contacts

Public ContactRamana Reddy MV

Gayatri Vidya Parishad Institute of Health Care and Medical Technology

drramanareddymoolagani@gmail.com9908232415

Outcome results

None listed

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