ClinicalTrials.gg
Status unknownNCT03371953Updated Dec 14, 2017

Evaluation of Atracurium-vecuronium Combination in Laparosocpic Surgery

A Phase 4 interventional study of Vecuronium and Atracurium in Patients Undergoing Laparoscopic Surgery, sponsored by Sir Ganga Ram Hospital. Status unknown at 1 site in India. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2017-12-14.

Sponsored by Sir Ganga Ram Hospital · Phase 4, Interventional, and Other

The sponsor has not verified this record recently (last verified Dec 2017), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 4
Study type
Interventional
Enrollment
48
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

Non-depolarising muscle relaxants are routinely employed to provide skeletal muscle relaxation during general anaesthesia (GA). Generally investigators use one or the other type of relaxant agent for this purpose and they are categorised based on their duration-of-action. Atracurium and vecuronium are two common muscle relaxant used during GA. They have an intermediate duration of action (around 40 minutes). Though they are effective relaxants and easy to reverse with reversal agents after the surgery, in case of the common laparoscopy procedures lasting an hour, they are relatively inefficient. There is evidence that when these agents are combined together (in 1:1 ratio), the duration-of-action, and reversibility improves. To render atracurium and vecuronium more efficient with laparoscopic surgery, the proposed study is aimed to evaluate the effects of combining 1/2 the respective standard doses of atracurium and vecuronium given together, in terms of its effect on the onset of block, duration-of-action, and reversibility of the neuromuscular blockade in adults undergoing laparoscopic surgery under GA. The study will be conducted with objective assessment parameter evaluation by TOF Watch SX (Organon, Teknica BV, Boxtel, The Netherlands), which will be used for facilitating institution, control, and monitoring the neuromuscular blockade during surgery. The objective of this study is to evaluate the additive effect of atracurium-vecuronium combination and profile its impact in patients undergoing laparoscopic surgery, especially in terms of increase in duration-of-action of muscle relaxation with the combination of drugs, when compared to respective individual drugs.

Read the detailed description

The principal pharmacological effect of neuromuscular blocking drugs is to interrupt the transmission of nerve impulses at the neuromuscular junction. They are classified into depolarising (mimics the action of acetylcholine) and non-depolarising (interfere with the action of acetylcholine).In general, we use vecuronium (0.08mg/kg) or atracurium (0.5mg/kg), which are intermediate-acting non-depolarising neuromuscular blocking agents for skeletal muscle relaxation.

The main use of neuromuscular blocking drugs is to provide skeletal muscle relaxation for facilitation of intubation of the trachea and to improve surgical working conditions in the anaesthetised patients. A 2×ED95 dose of non-depolarising muscle relaxant is recommended to facilitate tracheal intubation. In practice, 90% suppression of the single twitch response is usually considered clinical evidence of adequate drug-induced skeletal muscle relaxation.

Laparoscopy has become the most preferred means of surgical access for a variety of procedures. There are many laparoscopic surgeries that last about an hour. But the duration-of-action of bolus (intubating) dose of atracurium or vecuronium when used alone is not sufficient to last for an hour. As a result, for surgeries lasting an hour(e.g. laparoscopic cholecystectomy, laparoscopic total extra-peritoneal repair, etc.), one either end up giving a top up (maintenance) dose of vecuronium/atracurium to extend muscle relaxation or withhold the add-on dose and continue with surgery towards completion. While in the former situation, the anaesthesiologist is required to wait for long even though the surgery is completed; in the latter, either the surgery gets disturbed due to patient's movement (e.g. coughing, bucking) or there may be associated hemodynamic activation, which requires deepening of anaesthesia plane; both harbinger for patient-related adversity.

There are studies which have evaluated the effect of combining two non-depolarizing neuromuscular relaxants on the profile of skeletal muscle relaxation pertinent to anaesthetic (tracheal intubation) and surgical conditions.Atracurium and vecuronium are the most common non- depolarizing muscle relaxants we routinely employ during general anaesthesia (GA). Till date, to our knowledge, there are a very few studies that have evaluated combination of atracurium and vecuronium given together.Though, the limited number of studies which analysed effects of combined neuromuscular relaxation with atracurium and vecuronium underlined that there is an additive effect, commented only on onset-of-action and reversibility of muscle relaxation effect. In addition, no study has yet evaluated the duration-of-action of atracurium- vecuronium combination in adults undergoing laparoscopic surgeries. Muscle relaxation is used for optimising laparoscopic operating conditions by preventing diaphragmatic movement due to irritation by the presence of pneumoperitoneum and achieving more intra-abdominal space for a particular intra-abdominal insufflation pressure. In this context, deeper than normally maintained level of neuromuscular blockade appears to be superior. The investigators contend that combining vecuronium and atracurium would not only facilitate increase in duration-of-action of the relaxation but also provide quality muscle relaxation for the duration of surgery.

The proposed study looks forward to analyse the effect of muscle relaxation profile of vecuronium-atracurium combination versus vecuronium-alone or atracurium-alone in patients undergoing laparoscopic surgery.

02

Conditions studied

  • Patients Undergoing Laparoscopic Surgery

Keywords

  • vecuronium
  • atracurium
  • combination
03

In context

Lead sponsor

Sir Ganga Ram Hospital is the lead sponsor of 30 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. I and II
  2. Laparoscopic surgeries likely to last for 1 hour duration

Exclusion criteria

Exclusion Criteria:

  1. Patient refusal
  2. III and IV
  3. History of to atracurium or vecuronium
  4. Alcoholism and drug addiction
  5. Neuromuscular disorders
  6. Neuropsychiatric patients
  7. Hepatic and renal disease patients
  8. Obese patients
  9. Abnormal airway anatomy
  10. Risk of oesophageal reflux
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ASA physical status

The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Phase
Phase 4
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
48 participants (estimated)

Study arms

  • Active comparator
    Vecuronium group

    Vecuronium 0.08 mg/kg will be administered at induction of anaesthesia for facilitating muscle relaxation

    Drug: Vecuronium

  • Active comparator
    Atracurium group

    Atracurium 0.6 mg/kg will be administered at induction of anaesthesia for facilitating muscle relaxation

    Drug: Atracurium

  • Active comparator
    Vecuronium-Atracurium group

    Vecuronium 0.04 mg/kg + atracurium 0.3 mg/kg will be administered at induction of anaesthesia for facilitating muscle relaxation

    Drug: Vecuronium + Atracurium

Interventions

  • A top-up dose of vecuronium will be administered when the TOF count is 1 on the accelerometer. However, if there is a diaphragmatic contraction which interferes with surgical procedure then a dose will be given irrespective of the TOF count.

  • A top-up dose of vecuronium will be administered when the TOF count is 1 on the accelerometer. However, if there is a diaphragmatic contraction which interferes with surgical procedure then a dose will be given irrespective of the TOF count.

  • DrugVecuronium + Atracurium

    Drug pages: Vecuronium · Atracurium

    A top-up dose of vecuronium + atracurium will be administered when the TOF count is 1 on the accelerometer. However, if there is a diaphragmatic contraction which interferes with surgical procedure then a dose will be given irrespective of the TOF count.

06

What researchers measure

Primary outcomes

  1. Duration-of-action of the intubating dose

    Duration of action will be calculated from the time the drug is administered till theTOF count is 1 on the accelerometer.

    Time frame: From the time of administration of (0-hours, baseline) till 60-minutes intraoperatively

Secondary outcomes

  1. Onset-of-action of muscle relaxation following intubating dose

    Onset-of-action will be calculated from the time the drug is administered till theTOF count is 0 on the accelerometer.

    Time frame: From the time of administration of (0-hours, baseline) till 5-minutes intraoperatively

  2. Qualitative intubating conditions.

    Quality of intubating condition will be assessed using 3-point modified Cooper's scale. The intubating conditions will be graded as excellent, good \& poor. 1. The scale "Intubating conditions following intubating dose of non-depolarizing muscle relaxant" is modified from Cooper's Scale. The scale's name is derived from the name of the investigator (Cooper R) who first used it. (Br J Anaesth 1992; 69: 269-73) 2. The Cooper Scale includes five major variable sets \[1. Laryngoscopy (Jaw Relaxation), 2.Vocal-cord position, 3. Vocal cord movement, 4. Reaction to intubation and/or cuff inflation 5. Movement of limbs/ coughing\] which are classified as poor, good or excellent. For ease of the study analysis, poor is scored '0', good is scored '1', and excellent is scored '2'. Therefore, each variable has subscale range of 0-2 and, five variables are together ranged as 0-10. 3. Each of the five subscale range, i. e. 0-2, are added up to gain a 'total scale range score' of 0-10.

    Time frame: From the time of administration of (0-hours, baseline) till 5-minutes intraoperatively

  3. Reversibility of muscle relaxant effect

    Time for complete reversal of effect of muscle relaxation will be determined from the time of administration of reversal agent till the the point when TOF ratio is 90-percent.

    Time frame: From the time of administration of (0-hours, baseline) till 5-minutes post administration

07

Study locations

1 site
  • Sir Ganga Ram Hospital
    New Delhi, Delhi 110060, India
    • Amitabh Dutta, MD, PGDHR · Contactduttaamiatbh@yahoo.co.in · 00919810848064
    • Palem Reshmika, MBBS · Contactreshmika.palem@gmail.com · 00919773587847
    • Amitabh Dutta, MD,PGDHR · Principal investigator
    • Palem Reshmika, MBBS · Sub investigator
    • Savitar Malhotra, MD · Principal investigator
    • Subhash Gupta, MD · Sub investigator
    • Jayashree Sood, MD, FFARCS · Sub investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 14, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03371953
Lead sponsor
Sir Ganga Ram Hospital
Responsible party
Amitabh Dutta (Senior Consultant & Professor, Sir Ganga Ram Hospital) — Principal investigator
First posted
Dec 13, 2017
Start date
Dec 20, 2017 (estimated)
Primary completion
Oct 25, 2018 (estimated)
Completion
Oct 25, 2018 (estimated)
Last update
Dec 14, 2017

Study contacts

Amitabh Dutta, MD,PGDHR
Contact
duttaamiatbh@yahoo.co.in
00919810848064
Palem Reshmika
Contact
reshmika.palem@gmail.com
00919773587847
Amitabh Dutta, MD,PGDHR
study chair · Sir Ganga Ram Hospital
Subhash Gupta, MD
study director · Sir Ganga Ram Hospital
Savitar Malhotra, MD
principal investigator · Sir Ganga Ram Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drugs tested here: Vecuronium · Atracurium

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