Skip to main content
MedPathMedPath Home
Clinical Trials/CTRI/2020/11/029442
CTRI/2020/11/029442
Not yet recruiting
Phase 4

Comparative Evaluation of the Peri-operative Efficacy of Immuno-nutritional and Protein Supplements as a Dietary Adjunct in Participants Undergoing Surgical Management of Oral Squamous Cell Carcinoma-A Prospective Randomized Double Blind Study.

Department of Oral and Maxillofacial Surgery0 sites0 target enrollmentTBD
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Department of Oral and Maxillofacial Surgery
Status
Not yet recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\. Participants of both the genders in the age group of 18\-70 years.
  • •2\. Participants with Oral Squamous Cell Carcinoma who will undergo surgical resection of the tumor.
  • •3\. Participants with Oral Squamous Cell Carcinoma who will undergo surgical resection of the tumor with chemotherapy and/or Radiotherapy.
  • •4\. Participants in whom the planned surgery will be performed for duration of 4\-6 hours.
  • •5\. Participants willing for study.

Exclusion Criteria

  • •1\. Participants who have upper arm deformities.
  • •2\. Participants who are declared inoperable and are planned for palliative cancer therapies like radiotherapy and chemotherapy.
  • •3\. Participants in whom upper limb skin/flap is used for reconstruction purpose.
  • •4\. Participants who are a recurrence case of oral squamous cell carcinoma.
  • •5\. Participants who have undergone previous major surgeries under GA.
  • •6\. Participants presently suffering from a condition other than oral squamous cell carcinoma that also requires surgical intervention.
  • •7\. Participants who have a Renal Disorders and risen levels of Serum Creatinine.
  • •8\. Participants who have uncontrolled Diabetes.
  • •9\. Participants in whom the surgery will be undertaken for more than 6 hours.
  • •10\. Participants with Severe Sepsis.

Outcomes

Primary Outcomes

Not specified

Similar Trials

Recruiting
Not Applicable
Comparison of the effects of adding drug fentanyl via two different routes in patients undergoing cataract surgeries.
CTRI/2018/04/013177Bhagat Phool Singh Government Medical College for Women
Not yet recruiting
Not Applicable
Which block out of erector spinae plane block and thoracic paravertebral block provides better postoperative analgesia in patients after breast cancer surgery
CTRI/2019/08/020945ady Hardinge Medical College
Completed
Phase 4
evobupivacaine and Levobupivacaine+Adrenalin in Pediatric Tonsillectomy Operations.Tonsillitis
ACTRN12617001167358Selcuk University Medical Faculty88
Not yet recruiting
Phase 4
Comparison of three different methods in Surgical extractions of partially eruptedMandibular Third Molars using Piezo-Surgery and Piezo-surgery with steroid injections or rubber drain.Health Condition 1: K011- Impacted teeth
CTRI/2023/06/054276MGM Dental College and Hospital
Not yet recruiting
Not Applicable
Comparison of post cataract surgery outcome in standard phacoemulsification versus newer femtosecond assisted cataract surgery machine in advanced cataract.
CTRI/2021/12/038887ENSAR