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Black Seed Oil in Treatment of Osteoarthritis

Primary Purpose

Osteo Arthritis Knee

Status
Completed
Phase
Not Applicable
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Black seed oil capsule
Placebo Black seed oil capsule
Sponsored by
Ramsar international campus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteo Arthritis Knee

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: unilateral or bilateral involvement of one or more joints for over 4 months, ability to walk ability to stay throughout the study period no history of underlying inflammatory disease (arthropathy / rheumatoid arthritis), absence of diabetes, no history of allergy to black seed absence of hyperuricemia (<338 umol/l) or history of gout, absence of recent injury and trauma to the joint with osteoarthritis, absence of intra articular injection of corticosteroids in the last 4 months, lack of sensitivity to NSAIDS, no underlying liver and kidney disease or history of peptic ulcer Or gastrointestinal bleeding, Congestive Heart Failure, hypertension, and hyperkalemia , no fever absence of obvious Complete Blood Count disorders, coagulopathy, hematologic or neurological disorders , no alcohol consumption Exclusion Criteria: pregnancy, breast feeding, pregnancy-related decision obesity (BMI> 30 kg /m2).

Sites / Locations

  • Ramsar international campus

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Black seed

Placebo

Arm Description

Black seed oil capsule taken orally

Placebo capsule taken orally

Outcomes

Primary Outcome Measures

Knee joint pain
Scoring the functional status of individuals' joints were evaluated by applying Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) .reduce pain is identified based on the mean for the first 5 WOMAC questions (from no pain to severe pain)
joint movement limitation
Scoring the functional status of individuals' joints were evaluated by applying Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Joint movement is determined based on the average of questions 0 to 24 (from no problem to severe limit).
joint dryness
Scoring the functional status of individuals' joints were evaluated by applying Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). the 6th and 7th questions were specified for joint dryness (from no dryness to severe limitation)

Secondary Outcome Measures

Full Information

First Posted
September 1, 2023
Last Updated
September 7, 2023
Sponsor
Ramsar international campus
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1. Study Identification

Unique Protocol Identification Number
NCT06029868
Brief Title
Black Seed Oil in Treatment of Osteoarthritis
Official Title
Improving the Process of Dryness, Limited Movement, and Joint Pain Using the Black Seed in Osteoarthritis: a Randomized, Double-blind, Placebo-controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
January 14, 2019 (Actual)
Primary Completion Date
June 20, 2019 (Actual)
Study Completion Date
February 12, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ramsar international campus

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Osteoarthritis is a continual illness of joints. We aim to investigate the effect of Nigella sativa oil in comparison with placebo on the reduction of osteoarthritis pain. This study is a double-blinded, randomized, controlled trial study, conducting in Vali-e-Asr Hospital in 2019, in Birjand, on patients with mild osteoarthritis. The Western Ontario and McMaster Universities Osteoarthritis Index is applied to score the functional status of participants' joints.
Detailed Description
This study was a randomized controlled trial. Regarding to the inclusion criteria, 110 osteoarthritis patients were included in this study based on clinical signs, physical examination and radiological signs. In the next step, a fully explanation was given to the participants around the conditions of conducting the research, and then the informed consent were collected. Subsequently, patients were randomly divided into two groups of recipients; black seed soft gel capsules (intervention) and placebo equally in accordance with demographic information. Furthermore, the two groups were randomly classified regarding to age, consequently the study population was divided into subgroups of categorized ages. Thereafter, an equal number of each subgroup was randomly selected and divided into two groups to take black seed and placebo. Therefore, the two groups were similar, but the exact membership of individuals in the groups were random. Due to the higher prevalence of osteoarthritis among women in the community, the number of female cases were higher. It should be noted that the experimenters as well as patients did not know who was receiving a particular treatment (Double-blinded study). Prior to commencing the study, participants were asked to take a regular 48-day course of anti-inflammatory therapy. The cases in the intervention group took 700 mg of black seed soft gel capsule once a day from Gorgan Essential Oil Pharmaceutical Company, and the control group were treated by placebo capsules in the same-color and shape of the drug, with a taste of rice bran. Moreover, questionnaires were filled to record demographic information of both groups including age, sex, history medication and diet. The condition of participants were evaluated twice before the treatment and 48 days after the onset of black seed. At the end of each period, joint pain scores, the range of activity, and the dryness of the joints of all patients were assessed, and their mean were measured. Data collection tools: Scoring the functional status of individuals' joints were evaluated by applying Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)[2]. The WOMAC questionnaire was published in the 1908s to assess osteoarthritis of hip and knee, which is a standard criterion for assessing the health status of patients' self-reported activity. Three criteria should be measured ranging between zero to 4 for each question, by the end of each evaluation period: reduce pain is identified based on the mean for the first 5 WOMAC questions (from no pain to severe pain), the 6th and 7th questions were specified for joint dryness (from no dryness to severe limitation),and Joint movement is determined based on the average of questions 0 to 24 (from no problem to severe limit).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteo Arthritis Knee

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
110 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Black seed
Arm Type
Experimental
Arm Description
Black seed oil capsule taken orally
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo capsule taken orally
Intervention Type
Dietary Supplement
Intervention Name(s)
Black seed oil capsule
Intervention Description
700 mg black seed soft gel capsule once a day from Gorgan Essential Oil Pharmaceutical Company,
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo Black seed oil capsule
Intervention Description
Placebo Black seed oil capsule
Primary Outcome Measure Information:
Title
Knee joint pain
Description
Scoring the functional status of individuals' joints were evaluated by applying Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) .reduce pain is identified based on the mean for the first 5 WOMAC questions (from no pain to severe pain)
Time Frame
48 days
Title
joint movement limitation
Description
Scoring the functional status of individuals' joints were evaluated by applying Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Joint movement is determined based on the average of questions 0 to 24 (from no problem to severe limit).
Time Frame
48 days
Title
joint dryness
Description
Scoring the functional status of individuals' joints were evaluated by applying Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). the 6th and 7th questions were specified for joint dryness (from no dryness to severe limitation)
Time Frame
48 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: unilateral or bilateral involvement of one or more joints for over 4 months, ability to walk ability to stay throughout the study period no history of underlying inflammatory disease (arthropathy / rheumatoid arthritis), absence of diabetes, no history of allergy to black seed absence of hyperuricemia (<338 umol/l) or history of gout, absence of recent injury and trauma to the joint with osteoarthritis, absence of intra articular injection of corticosteroids in the last 4 months, lack of sensitivity to NSAIDS, no underlying liver and kidney disease or history of peptic ulcer Or gastrointestinal bleeding, Congestive Heart Failure, hypertension, and hyperkalemia , no fever absence of obvious Complete Blood Count disorders, coagulopathy, hematologic or neurological disorders , no alcohol consumption Exclusion Criteria: pregnancy, breast feeding, pregnancy-related decision obesity (BMI> 30 kg /m2).
Facility Information:
Facility Name
Ramsar international campus
City
Ramsar
State/Province
Mazandaran
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

Plan to Share IPD
No

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Black Seed Oil in Treatment of Osteoarthritis

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