NCT03520595

Brief Summary

Introduction: Homeopathy is a deep healing, comprehensive and distinct system originally developed by Samuel Hahnemann about 200 years ago. Small doses of specially prepared ("potentized") remedies which set the body's systems back in order and stimulate a body's own energies toward a natural healing process. It is entirely distinct in both theory and in practice from other healing systems from ordinary or main-stream ("allopathic") medicine, but also from acupuncture, naturopathy, chiropractics, etc., although some homeopathy often finds its way into these other fields of practice.Homeopathy is based on the concept "similia similibus curentur" which means symptoms, caused by the original substance in healthy subjects, can be reversed by the homeopathic remedy in patients having similar symptoms.Homeopathy has the advantages such as it is inexpensive (the only expense is the homeopath's time and training - the remedies themselves cost practically nothing), non-toxic (although "side affects" which reflect the body's own healing processes may occur - such as fever, discharge, rash, etc.) and non-intrusive (the remedies are carried on tiny sugar granules which are dissolved in water or in the mouth, or swallowed).Arnica is one of the most popular medications in homeopathy medicine. This remedy can be extracted from several plant species belonging to the Aesteraceae family including Arnica montana, Arnica fulgens, Arnica cordifolia, Arnica chamissonis and Arnica sororia, and it is widely sold as tincture, ointment, cream, gel, and tablet. It has been used for the treatment of numerous pathological conditions, including pain, swelling and stiffness associated with trauma, contusions, sprains, myocarditis, angina pectoris, cardiac insufficiency, arteriosclerosis, postoperative clinical conditions, and for symptomatic relief in osteoarthritis.Conventional NSAIDs work by inhibiting cyclooxygenase (COX) and prostaglandin synthesis as well as by other less understood mechanisms. Onset of analgesia occurs rapidly with all NSAIDs, usually within one hour.Diclofenac is one of potent, standard and most unique NSAID for the therapy of postoperative pain. Diclofenac inhibits the lipoxygenase pathways, which reduces the formation of the leukotrienes (also pro-inflammatory autacoids) and also inhibit phospholipase A2. These actions explain the high potency of diclofenac.NSAIDs cause a variety of side effects including nausea, diarrhea, constipation, dizziness, headache, confusion, edema, rash, and pruritis. They can also cause more serious toxicities such as gastrointestinal (GI) ulceration/bleeding, hematologic disturbances, bronchospasm, angioedema, renal dysfunction, and hepatotoxicity. Many of these side effects are due to NSAID inhibiting prostaglandin synthesis other than at the desired site of action.Arnica being clinical efficient and high tolerable makes it a potential therapeutic alternative target to non-steroidal anti-inflammatory drugs.In this study investigator will compare and evaluate the efficacy of Arnica as a substitute for analgesics such as Diclofenac Sodium, through which side effects of NSAIDS can be avoided and get the same analgesia effect through Arnica without any of the undesirable effects for minor surgical procedures. AIM: To compare and evaluate the analgesic effect of Arnica Montana with Diclofenac sodium after crown lengthening procedure with ostectomy. Objectives: To assess the analgesic effect on crown lengthening procedure with ostectomy patients of Arnica Montana and Diclofenac Sodium.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2016

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2016

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 31, 2017

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2017

Completed
8 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 8, 2017

Completed
1.3 years until next milestone

First Posted

Study publicly available on registry

May 11, 2018

Completed
Last Updated

May 15, 2018

Status Verified

May 1, 2018

Enrollment Period

2 months

First QC Date

January 31, 2017

Last Update Submit

May 9, 2018

Conditions

Outcome Measures

Primary Outcomes (1)

  • Visual Analog Scale

    Pain Assessment is done by visual analog scale which consists of 10 centimeter line. anchored by two extremes starting from 1 ending to 10, of which 1 being the lowest and 10 being highest score.

    3 days

Study Arms (3)

Arnica Group

ACTIVE COMPARATOR

Study group 1 CLP with ostectomy Arnica 200 drug 3 pills,3 times daily for 3 days

Drug: Arnica 200 drug 3 pills,3 times daily for 3 days

Diclofenac Sodium group

ACTIVE COMPARATOR

Study group 2 CLP with ostectomy Diclofenac Sodium 50mg twice daily after meals with plain water

Drug: Diclofenac Sodium 50mg twice daily

Placebo Group

PLACEBO COMPARATOR

Study group 3 CLP with ostectomy Placebo pills and distilled water 3 pills,3 times daily

Drug: Placebo pills and distilled water 3 pills,3 times daily

Interventions

CLP with ostectomy done in patients whose biologic width and crown height is insufficient

Also known as: CLP with ostectomy
Arnica Group

CLP with ostectomy done in patients whose biologic width and crown height is insufficient

Also known as: CLP with ostectomy
Diclofenac Sodium group

CLP with ostectomy done in patients whose biologic width and crown height is insufficient

Also known as: CLP with ostectomy
Placebo Group

Eligibility Criteria

Age17 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Systemically healthy patients.
  • Patients with inadequate crown height for replacement for prosthesis.

You may not qualify if:

  • Tobacco intake in any form and alcohol.
  • Pregnant \& lactating women.
  • Any known/reported allergy to given drugs.
  • On Antibiotics medications.
  • Patient with the history of acidity ,gastric disorders.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dental

Kolhāpur, Maharashtra, 416113, India

Location

MeSH Terms

Interventions

cysteine and glycine-rich protein 3Diclofenac

Intervention Hierarchy (Ancestors)

PhenylacetatesAcids, CarbocyclicCarboxylic AcidsOrganic Chemicals

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

January 31, 2017

First Posted

May 11, 2018

Study Start

December 1, 2016

Primary Completion

January 31, 2017

Study Completion

February 8, 2017

Last Updated

May 15, 2018

Record last verified: 2018-05

Locations