To Assess The Main Out Come Of Intra Operative Infusion Of Lignocaine On Post Operative Pain,Nausea Vomiting And Recovery In Participants Undergoing Laproscopic Gynecologycal Procedures

To Evaluate The Efficacy Of Intra Operative Infusion Of Lignocaine On Post Operative Pain, Nausea, Vomiting And Recovery In Patients Undergoing Laparoscopic Gynecological Procedures - Nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/069758

Enrollment

Registered

2024-07-01

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

Health Condition 1: N946- Dysmenorrhea, unspecified

Interventions

Intervention1: Intravenous Infusion Of Drug In Controlled Group And Normal Saline In Placebo Group: Patient Will Receive Preservative Free Lignocaine 2% 1.5ml/Kg/Iv Bolus Over 10min Before Endotrachea

Eligibility

Inclusion criteria

Inclusion criteria: Patient Belonging To Asa 1-2 Patient Undergoing Elective Laproscopic Gynecological Surery Under General Anesthesia Less Than 2 Hours

Exclusion criteria

Exclusion criteria: Pregnant Woman Patient Allergic To Local Anaesthetic Patient Refusal for Study

Design outcomes

Primary

Measure	Time frame
To Asesess Numerical Rating Scale For Post Operative Pain To Estimate The Lenght Of Stay In Post Operative Care Unit To Evaluate Post Operative Nausea And Vomiting Timepoint: Post Operative Hemodynamic Parameters From Arrival To Pacu ,Every 15min Till 1 Hour	—

Secondary

Measure	Time frame
To Identify First Request For Post Operative Analgesia Total Analgesia Consumption Timepoint: Antiemetics Requirments 24 Hours Time Of 1st Analgesia Total Analgesia In 24hours	—

Countries

India

Contacts

Public ContactShushritha N

Vydehi Institute Of Medical Science And Research Centre

shushrithan27@gmail.com8971719762

Outcome results

None listed

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